Weekly Recall Recap

NewerOlder

2026-05-25 to 2026-05-31

131
Recalls
589,738
Units
10
Injuries
0
Deaths

Sources: NHTSA, CPSC, FDA_FOOD, FDA_DEVICE, FDA_DRUG

Other Recalls

NHTSA2026-05-2970 units
Wheelchair Restraint Retractor May Not Lock
ARBOC Specialty Vehicles, LLC

An unsecured wheelchair can move during transit, increasing the risk of injury.

NHTSA2026-05-29125 units
Drive Motor May Detach
International Motors, LLC

A detach drive motor can become a road hazard for other vehicles, increasing the risk of a crash or injury.

NHTSA2026-05-29644 units
Do Not Drive: Wheel May Detach
Mack Trucks, Inc.

Wheel detachment can cause a loss of vehicle control or create a road hazard, increasing the risk of a crash or injury.

NHTSA2026-05-29155 units
Do Not Drive: Wheel May Detach
Volvo Trucks North America

Wheel detachment can cause a loss of vehicle control or create a road hazard, increasing the risk of a crash or injury.

NHTSA2026-05-28277 units
Wheelchair Restraint Retractor May Not Lock
Forest River Bus, LLC

An unsecured wheelchair can move during transit, increasing the risk of injury.

NHTSA2026-05-2881,893 units
Instrument Panel Display Failure/FMVSS 101, 305
Toyota Motor Engineering & Manufacturing

An instrument panel display that fails to show critical safety information, such as engine coolant temperature or electrical charge increases the risk of a crash or injury.

NHTSA2026-05-2869,663 units
Moonroof Glass May Detach
Subaru of America, Inc.

A detached glass panel may become a road hazard, increasing the risk of a crash.

NHTSA2026-05-281,536 units
Loss of Drive Power from Engine Failure
Ford Motor Company

A sudden loss of drive power can increase the risk of a crash.

NHTSA2026-05-28419,967 units
Seat Belt May Fail to Retract or Extend
Ford Motor Company

Seat belts that do not retract or extend can fail to restrain an occupant as intended, increasing the risk of injury in a crash.

NHTSA2026-05-28232 units
Incorrect Gear May Be Selected
General Motors, LLC

Inaccurate gear selection may result in unexpected vehicle movement, increasing the risk of a crash.

CPSC2026-05-28
Walmart Recalls Mainstays 9-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Hop Thang Interior Wood Co. Ltd., of Vietnam

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.

CPSC2026-05-28
Joy Furniture Recalls Talan and Royce Living Room Furniture Sets Due to Risk of Serious Injury from a Fire Hazard
Zhejiang Mingrui Furniture Co. Ltd. aka Joy Furniture

The LED lights on the recalled illuminated spheres can overheat, posing a risk of serious injury or death from a fire hazard.

CPSC2026-05-28
Lithium Coin Batteries Recalled Due to Battery Ingestion; Violates Federal Statute for Child-Resistant Packaging of Coin Batteries; Imported by Proudly American Store, of Canada

The recalled coin batteries are not in child-resistant packaging and do not bear the warning labels required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

CPSC2026-05-28
Luminous Fidget Spinner Balls Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Anzmtosn
Shenzhenshibangduoladianzikejimaoyi Co., Ltd (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), doing business as Anzmtosn, of China

The recalled toys violate the?mandatory safety standard for toys?because the mini flashlight included with the fidget spinner balls contains button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries,?including internal chemical burns, and death.

CPSC2026-05-28
MiniWarGaming and Primal Horizon Disc Magnets Recalled Due to Risk of Serious Injury or Death from Ingestion; Violate Mandatory Standard for Magnets; Imported by MiniWarGaming

The magnets violate the mandatory safety standard for magnets because the high-powered magnets fit within CPSC's small parts cylinder and are stronger than permitted, posing a deadly ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

CPSC2026-05-28
Missry Associates Recalls Misco Sports Light-Up Racket Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys

The racket sets violate the mandatory standard for toys because the screw on the racket used to secure the battery compartment does not remain attached when opened, and the button cell batteries in the shuttlecock can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

CPSC2026-05-28
Tzumi Electronics Recalls SLF Sauna Blankets Due to Fire and Burn Hazards

The recalled sauna blankets can overheat, posing fire and burn hazards.

NHTSA2026-05-28160 units
Incorrectly Colored Cargo Carrying Capacity Label/FMVSS 120
Tiffin Motorhomes, Inc.

The incorrect label color may make it difficult for the operator to locate the loading or tire pressure information, increasing the risk of a crash.

CPSC2026-05-28
Giantex Recalls Giantex and Costway Portable Steam Saunas Due to Burn Hazard

The sauna's steam diffuser can be positioned too close to a consumer's body, allowing hot steam to come in contact with user, posing a burn hazard.

CPSC2026-05-28
Giantex Recalls Lounge Chairs Due to Amputation Hazard

Consumers can place their fingers in a pinch point, when adjusting the lounge chair, posing an amputation risk.

CPSC2026-05-28
Daoen Recalls Zen Magnetic Promotional Ball Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys

The recalled magnetic balls violate the mandatory standard for toys because they are loose high-powered magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, they can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

NHTSA2026-05-274,653 units
Do Not Drive: Loss of Control from Control Arm Separation
Ford Motor Company

A detached control arm can cause a loss of vehicle control, increasing the risk of a crash.

FDA Food2026-05-27
FDA Recall: Menopause Bully 16 oz and 32 oz.
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: Solina 6036195 Ranch Seasoning, 50lb bag
Solina U.S. Holding

potential to be contaminated with Salmonella

FDA Food2026-05-27
FDA Recall: Liposomal B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: Vitam
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients:
Ghirardelli Chocolate Company

Potential contamination with Salmonella.

FDA Food2026-05-27
FDA Recall: Solina 6036087 Cr¿me Fraiche Spice Seasoning, 25lb bag
Solina U.S. Holding

potential to be contaminated with Salmonella

FDA Food2026-05-27
FDA Recall: Solina 6036277 Garlic Cream Sauce Seasoning, 40lb bag
Solina U.S. Holding

potential to be contaminated with Salmonella

FDA Food2026-05-27
FDA Recall: Liposomal Kids Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Fir
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: Solina 6036554 Parmesan Breadstick Sauce Seasoning, 40lb bag
Solina U.S. Holding

potential to be contaminated with Salmonella

FDA Food2026-05-27
FDA Recall: Fibroid Bully 16 oz and 32 oz.
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX WHITE MOCHA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: ***
Ghirardelli Chocolate Company

Potential contamination with Salmonella.

FDA Food2026-05-27
FDA Recall: Solina 6022487 Garlic Herb Topping, 50lb bag
Solina U.S. Holding

potential to be contaminated with Salmonella

FDA Food2026-05-27
FDA Recall: Squirrel Brand Town & Country Mix 16 oz can UPC 07223805251 and 7.5 oz can UPC 07223805450. 16 oz 1
JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

FDA Food2026-05-27
FDA Recall: Immunity Enhancer Elderberry 16 oz and 32 oz.
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET mode
Llorens Pharmaceuticals International Division, Inc.

Foreign object: black particulate matter

FDA Food2026-05-27
FDA Recall: Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: Vi
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: Liposomal Women's Liquid Multivitamin Drops - Iron Free. Dosage: 3ml Liquid. Packaging: Aluminum bot
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: Sea Moss Tonic 16 oz and 32. oz.
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.42kg Ingredient
Ghirardelli Chocolate Company

Potential contamination with Salmonella.

FDA Food2026-05-27
FDA Recall: Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml Liquid. Packaging: Aluminum bottle. 90 m
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

NHTSA2026-05-27143 units
Improperly Tightened Shock Bolts
Ember Recreational Vehicles, INC

Broken shock retainer bolt heads and washers may detach and become a road hazard, increasing the risk of a crash.

NHTSA2026-05-27392 units
Park Outside: Fuel Tank Puncture May Cause Fire
Tiffin Motorhomes, Inc.

A fuel leak in the presence of an ignition source, increases the risk of a fire.

FDA Food2026-05-27
FDA Recall: Squirrel Brand Travelers Mix 16 oz can UPC 07223899166, 12 cans per case
JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

FDA Food2026-05-27
FDA Recall: Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address:
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113. Net Wt 25.00 lbs (11.3kg). PS Seasonin
PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

FDA Food2026-05-27
FDA Recall: GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.41kg Distributed
Ghirardelli Chocolate Company

Potential contamination with Salmonella.

FDA Device2026-05-27
FDA Recall: Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmo
Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

FDA Food2026-05-27
FDA Recall: GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 10lbs (4.54kg) Ingredients: *** n
Ghirardelli Chocolate Company

Potential contamination with Salmonella.

FDA Drug2026-05-27
FDA Recall: Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in cartons of 10
Safecor Health, LLC

Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.

FDA Drug2026-05-27
FDA Recall: fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compound
IntegraDose Compounding Services LLC

Subpotent Drug

FDA Drug2026-05-27
FDA Recall: Erythromycin Tablets, USP, 500 mg, 30 tablets per bottle, Rx only, Manufactured by: Zydus Lifescienc
Zydus Pharmaceuticals (USA) Inc

CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit

FDA Drug2026-05-27
FDA Recall: Liraglutide Injection, 18 mg/3 mL (6 mg/mL), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.,
Lupin Pharmaceuticals Inc.

Presence of particulate matter: a white thread-like structure in the cartridge

FDA Drug2026-05-27
FDA Recall: Erythromycin Tablets, USP, 250 mg, 30 tablets per bottle, Rx only, Manufactured by: Zydus Lifescienc
Zydus Pharmaceuticals (USA) Inc

CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit

FDA Drug2026-05-27
FDA Recall: Primidone Tablets, USP, 50 mg, 100 Tablets (10 x 10 unit dose blister) per carton, Rx only, Distribu
Amerisource Health Services LLC

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

FDA Drug2026-05-27
FDA Recall: Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Mar
Golden State Medical Supply Inc.

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

FDA Drug2026-05-27
FDA Recall: Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., M
Golden State Medical Supply Inc.

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

FDA Drug2026-05-27
FDA Recall: MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%), NET WT 6 oz (170 g), M
Wisconsin Pharmacal Company

Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.

FDA Drug2026-05-27
FDA Recall: cimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by
UCB Biosciences Inc.

Lack of Assurance of Sterility

FDA Drug2026-05-27
FDA Recall: Primidone Tablets, USP, 250 mg, 100 Tablets (10 x 10 unit dose blister) per carton, Rx only, Distrib
Amerisource Health Services LLC

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

FDA Drug2026-05-27
FDA Recall: Estradiol Gel, 0.1%, 0.25 mg, 0.25 g per packet, 30 packets per carton, Rx only, Distributed by: ANI
ANI Pharmaceuticals, Inc.

Defective Container; packets were found to be either empty or partially full.

FDA Food2026-05-27
FDA Recall: Pork King Good Onion & Sour Cream Seasoning. Net Wt. 3 oz (85G) bottle. UPC 8 50008-53861 2. Made
Pork King Good, LLC

Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination.

FDA Food2026-05-27
FDA Recall: Liposomal Collagen Booster. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vit
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: Liposomal Women's Liquid Multivitamin Drops with Iron. Dosage: 3mL Liquid. Packaging: Aluminum bottl
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

NHTSA2026-05-272,622 units
Incorrectly Tightened Shock Bolts
Alliance RV, LLC

Broken shock retainer bolt heads and washers may detach and become a road hazard to other vehicles, increasing the risk of a crash.

FDA Food2026-05-27
FDA Recall: Solina 6036786 Instant Country Gravy Seasoning, 40lb bag
Solina U.S. Holding

potential to be contaminated with Salmonella

FDA Food2026-05-27
FDA Recall: Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral use. Packaging: Plastic Bottle. Net Vol
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns.

FDA Drug2026-05-27
FDA Recall: Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Phil
Lannett Company Inc.

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

FDA Device2026-05-27
FDA Recall: Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75
Becton, Dickinson and Company

Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

FDA Device2026-05-27
FDA Recall: Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P
Becton, Dickinson and Company

Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

FDA Device2026-05-27
FDA Recall: Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (7220
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.

FDA Device2026-05-27
FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary
Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

FDA Device2026-05-27
FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary
Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

FDA Device2026-05-27
FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonar
Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

FDA Food2026-05-27
FDA Recall: Non Fat Dry Milk 1#, Part #: 02000014P. Net Wt 1 lb (453g) PS Seasoning & Spices 216 W Pleasant St
PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

FDA Food2026-05-27
FDA Recall: Solina 6035687 Bayou Blackened Ranch Seasoning, 25lb bag
Solina U.S. Holding

potential to be contaminated with Salmonella

FDA Food2026-05-27
FDA Recall: MA Cohen's Kippered Herring vacuum packed, weight provided at retail, UPC 7232577992
Shining Sea Fish Co. LLC

Clostridium botulinum is an uncontrolled hazard

FDA Food2026-05-27
FDA Recall: FulviLife Complex. Dosage:2 tablespoons (30mL). Liquid. Packaging: Plastic Bottle. Net Volume:16 fl
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: GHIRARDELLI PREMIUM HOT COCOA MIX NET WT 32oz (2lbs) 907g Ingredients: *** nonfat dry milk *** Dist
Ghirardelli Chocolate Company

Potential contamination with Salmonella.

FDA Device2026-05-27
FDA Recall: Swan-Ganz Pacing Catheter, Models: D200F7;
Becton, Dickinson and Company

Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

FDA Device2026-05-27
FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary
Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

FDA Device2026-05-27
FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary
Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

FDA Food2026-05-27
FDA Recall: PSW21585 Save A Lot Bind 50#, Part #: 20009709. PS Seasoning & Spices 216 W Pleasant St Iron Ridge
PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

FDA Food2026-05-27
FDA Recall: C0017D Natural & Artificial White Cheddar Cheese Flavor, Net Weight: 50 lbs. bag. Item #: 8500101
Fontana Flavors, Inc

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

FDA Food2026-05-27
FDA Recall: C7139D1 Natural Parmesan Cheese Flavor, Net Weight: 50 lbs. bags. Item #: 202405. For Further Pr
Fontana Flavors, Inc

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

FDA Food2026-05-27
FDA Recall: Blood Pressure Bully 16 oz and 32 oz
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CLASSIC WHITE NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: **
Ghirardelli Chocolate Company

Potential contamination with Salmonella.

FDA Food2026-05-27
FDA Recall: GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX MOCHA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat
Ghirardelli Chocolate Company

Potential contamination with Salmonella.

FDA Food2026-05-27
FDA Recall: Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240, 8 bags per case
JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

FDA Food2026-05-27
FDA Recall: VG7274D1 Natural Cream of Mushroom Type Flavor, Net Weight: 50 lbs. bag. Item #: R5302. For Fu
Fontana Flavors, Inc

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

FDA Food2026-05-27
FDA Recall: Fisher Tex Mex Trail Mix 30 oz plastic jar UPC 070690275941, 6 jars per case
JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

FDA Food2026-05-27
FDA Recall: Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: Vit
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: Solina 6036443 Cheddar Cheese Powder Seasoning, 50lb bag
Solina U.S. Holding

potential to be contaminated with Salmonella

FDA Food2026-05-27
FDA Recall: Blackstone Parmesan Ranch Seasoning, Net Wt 7.3 oz (207g). UPC 7 17604-04106 2. Manufactured for N
PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

FDA Food2026-05-27
FDA Recall: Prostate Bully 16 oz and 32 oz
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: Blackseed Bitters 16 oz and 32 oz.
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: Pure Shilajit Tonic 16 oz and 32 oz
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: GHIRARDELLI SWEET GROUND POWDER CHOCOLATE & COCOA NET WT 48oz (3lbs) 1.36kg Distributed by Ghirarde
Ghirardelli Chocolate Company

Potential contamination with Salmonella.

FDA Food2026-05-27
FDA Recall: Liposomal Mens 50+ Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml.
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 oz plastic jar UPC
JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

FDA Food2026-05-27
FDA Recall: Southern Style Nuts Hunter Mix 30 oz plastic jar UPC 085839916302, 4 jars per case
JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

FDA Food2026-05-27
FDA Recall: Liposomal Prenatal+Postnatal Liquid Multivitamin Drops - Iron Free. Dosage: 3mL Liquid. Packaging: A
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX VANILLA NET WT 48oz (3lbs) 1.36kg Ingredients: *** nonfat d
Ghirardelli Chocolate Company

Potential contamination with Salmonella.

FDA Food2026-05-27
FDA Recall: Stoltzfus Family Farm Sour Cream and Onion cheese curds, 8-ounce
Stoltzfus Family Dairy LLC

Product may be contaminated with Salmonella.

FDA Food2026-05-27
FDA Recall: Liquid Blenz Good Brain Tonic 16 oz and 32 oz
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Fi
Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

FDA Food2026-05-27
FDA Recall: YT 6027393 Spicy Ranch Blend, 50lb bag
Solina U.S. Holding

potential to be contaminated with Salmonella

FDA Food2026-05-27
FDA Recall: Pure Diabetes Bully 16 oz and 32 oz.
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: Liquid Blenz Soursop Bitters 16 oz and 32 oz.
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: Flat Belly Bully 16 oz and 32 oz
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Food2026-05-27
FDA Recall: 1P Original Smokehouse Unit for 300 lbs. of Meat, Part #: 180002964. Net Wt 15.10 lbs (6.85kg). PS
PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

FDA Food2026-05-27
FDA Recall: Solina 6035415 Sourdough Cheese Crouton Seasoning, 50lb bag
Solina U.S. Holding

potential to be contaminated with Salmonella

FDA Food2026-05-27
FDA Recall: 1P Jalapeno Heat Unit for 300 lbs of Meat, Part #: 180002945. Net Wt 18 lbs (8.20kg). PS Seasoni
PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

FDA Food2026-05-27
FDA Recall: Pure Libido Drink 16 oz and 32 oz.
LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

FDA Drug2026-05-27
FDA Recall: Busulfan Injection, 60 mg per 10 mL (6 mg per mL), 8x10 mL Single-Dose Vials, Rx only, Mfd. for Sage
Sagent Pharmaceuticals

Failed Impurities/Degradation Specifications

FDA Drug2026-05-27
FDA Recall: Gas-X, Simethicone 125 mg/ ANTIGAS, 120 SoftGels, Distributed by: Haleon, Warren, NJ 07059, UPC: 3 0
Haleon US Holdings LLC

Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling.

FDA Drug2026-05-27
FDA Recall: Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid, Contains: Folic Acid 799 m
Safecor Health, LLC

Presence of a Foreign Substance; black particles observed in liquid

FDA Device2026-05-27
FDA Recall: Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below pro
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.

FDA Device2026-05-27
FDA Recall: OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Sm
Novapproach Spine, LLC

Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, which could lead to procedural delay and/or the need to select an alternative implant.

FDA Device2026-05-27
FDA Recall: Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 3342
C.R. Bard Inc

Due to stain present on the surface of affected foley catheters.

FDA Device2026-05-27
FDA Recall: Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TN
TANGENT ENDOSCOPY, LLC

Affected devices exhibited fractures at the distal shaft tip without complete detachment.

FDA Device2026-05-27
FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Cardiopulmonary
Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

FDA Device2026-05-27
FDA Recall: Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-N
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.

FDA Device2026-05-27
FDA Recall: Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.

FDA Device2026-05-27
FDA Recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonar
Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

FDA Device2026-05-27
FDA Recall: Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valv
ICU Medical, Inc.

Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs during therapy this may result in therapy interruption with the potential for the patient to receive less infusion solution than intended. Exposure of hazardous substances to the patient, caregiver, or pharmacy technician is possible.

FDA Device2026-05-27
FDA Recall: Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmona
Medtronic Perfusion Systems

Certain lots of product have the potential for a sterile barrier breach.

NHTSA2026-05-26268 units
Incorrect Tire and Weight Capacity Information/FMVSS 110
Ford Motor Company

The incorrect tire size, tire pressures, and GAWR listed on the labels can allow the vehicle to be overloaded or have improperly inflated tires, increasing the risk of a crash.

NHTSA2026-05-26677 units
Wheelchair Restraint Retractor May Not Lock
Coach and Equipment Mfg. Corp.

An unsecured wheelchair can move during transit, increasing the risk of injury.

NHTSA2026-05-26200 units
Incorrectly Tightened Shock Bolts
Forest River, Inc.

Broken shock retainer bolt heads and washers may detach and become a road hazard for other vehicles, increasing the risk of a crash.

NHTSA2026-05-266,061 units
Incorrectly Tightened Shock Bolts
Brinkley RV

Broken shock retainer bolt heads and washers may detach and become a road hazard for other vehicles, increasing the risk of a crash.