Weekly Recall Recap

NewerOlder

2026-08-24 to 2026-08-30

113
Recalls
2,400,508
Units
0
Injuries
0
Deaths

Sources: FDA_FOOD, NHTSA, CPSC, FDA_DEVICE, FDA_DRUG

Other Recalls

FDA Food2026-08-29
FDA Recall: Everything Sprouts: Robust Radish Mix, 5oz Cups
Everything Sprouts

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

FDA Food2026-08-29
FDA Recall: Martina: Mangoes
Martina

Potential contamination with Salmonella

FDA Food2026-08-28
FDA Recall: Northwest Naturals: Chicken Recipe
Northwest Naturals

Potential contamination with Salmonella and/or Listeria monocytogenes

NHTSA2026-08-288 units
Incorrect GAWR on Certification Label
Jayco, Inc.

Referencing the incorrect weight could result in the trailer being overloaded, increasing the risk of a crash.

CPSC2026-08-271,905,805 units
Conair Expands Recall of Cuisinart Grill Brushes Due to Ingestion Hazard; Over 3.6 Million Brushes Now Recalled
Conair LLC of Stamford, Connecticut

Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.

CPSC2026-08-27165,250 units
Walmart Reannounces Recall of Mainstays Nine-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Walmart Distributed Recalled Dressers Post-Recall; Sold to Consumers Through Liquidators
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.

NHTSA2026-08-27280 units
Strobe Light May Short Circuit
Altec Industries, Inc.

An electrical short-circuit can increase the risk of a fire.

NHTSA2026-08-2723 units
Improperly Tightened Vehicle Joints
Ford Motor Company

Improperly tightened vehicle joints may lead to a loss of vehicle control, electrical failure, or detached parts, increasing the risk of a crash or fire.

CPSC2026-08-27243 units
Kmaier Recalls Infant Walkers Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers
FENUN, Inc., dba Kmaier, of Pasadena, California

The recalled walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a deadly fall hazard.

CPSC2026-08-272,000 units
HABA USA Recalls Rainbow Rattle Grasping and Teething Toys Due to Risk of Serious Injury or Death from Choking and Ingestion Hazards
Habermaass Corporation, Inc. dba HABA USA, of Skaneateles, New York

The glued knot on the elastic cord can become untied on the recalled product, allowing young children access to the small wooden and plastic pieces, posing a risk of serious injury or death from choking and ingestion hazards.

CPSC2026-08-2755,250 units
Diamond Wipes International Recalls MD Wipe Outz Numbing Tattoo Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Diamond Wipes International, Inc., of Chino, California

The recalled numbing wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of the wipes is not child-resistant, posing a risk of serious injury or death from poisoning if the contents of the wipes are ingested by young children.

CPSC2026-08-2790 units
AudioLineOut Recalls Studio Six Headphone Amplifiers Due to Risk of Serious Injury or Death from Electrocution Hazard
AudioLineOut LLC, of Portland, Oregon

When the amplifiers are used with aftermarket metal base tubes, the bare metal can become electrified, posing a risk of serious injury or death from electrocution.

CPSC2026-08-271,800 units
Excel Industries Recalls Accessory LED Light Kits Due to Risk of Serious Injury from Fire Hazard
Excel Industries LLC, of Hesston, Kansas

The light bars can overheat or produce flames, posing a risk of serious injury from a fire hazard.

CPSC2026-08-27128 units
Steelite Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by Longer 3D
Longer Technology (Hong Kong) Limited, dba Longer 3D, of China

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing a risk of serious injury or death from shock and electrocution hazards.

CPSC2026-08-27590 units
Little Loves & Co. Recalls Youth Clothing with Drawstrings Due to Risk of Serious Injury or Death from Entrapment Hazard
Little Loves & Co. LLC, of Olympia, Washington

The drawstrings in the recalled clothing can get caught on objects and cause death or serious injury to children due to an entrapment hazard.

CPSC2026-08-27300 units
Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by YERYORK
Lanzhou Xinshi Mingchen Information Technology Co., Ltd., dba YERYORK, of China

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of injury or death from shock and electrocution hazards.

CPSC2026-08-2720,134 units
Montessori Baby Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Chillife Official
Shenzhenshixingchuangyiyimaoyouxiangongsi (Shenzhen Xingchuangyi Trading Co., Ltd.) dba Chillife Official, China.

The recalled baby toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The silicone strings can reach the back of children’s throat and become lodged, posing a risk of respiratory distress and deadly choking hazard.

NHTSA2026-08-27400 units
Helmets with Inadequate Impact Protection/FMVSS 218
Bell Sports, Inc.

A helmet that does not provide adequate impact protection increases the risk of injury in a crash.

FDA Food2026-08-26
FDA Recall: Shelter’s Choice, Breeder’s Edge: Feline Milk Replacers
Shelter’s Choice, Breeder’s Edge

Low levels of potassium, copper, folic acid, choline and/or pyridoxine (vitamin B6)

NHTSA2026-08-2610,001 units
Improperly Manufactured Pistons May Fail
Ford Motor Company

An unexpected loss of drive power increases the risk of a crash.

FDA Food2026-08-26
FDA Recall: Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn 3.5oz
Prospector Popcorn, LLC

Inaccurately declared nutrients including Iron (understated), and Vitamin D (overstated).

FDA Device2026-08-26
FDA Recall: Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (530390
AVID Medical, Inc.

The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.

FDA Food2026-08-26
FDA Recall: Whole Foods Pomegranate Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic con
WFM Purchasing, LP

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

FDA Drug2026-08-26
FDA Recall: ACETYLCYSTEINE SOLUTION, USP, 10% (100 mg/mL), packaged in a) 4 mL Vial NOT FOR INJECTION (NDC 0517-
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Food2026-08-26
FDA Recall: Protein Cereal Cocoa Crunch. Shelf stable, ready to eat cereal product. 25-year shelf life, metalize
Nutrient Foods, LLC

Soy not declared in the contains statement.

FDA Device2026-08-26
FDA Recall: American Contract Systems medical procedure kits and trays labeled as: 1) ANTERIOR CERVICAL PACK
American Contract Systems Inc

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.

FDA Device2026-08-26
FDA Recall: MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW
Medtronic MiniMed, Inc.

Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.

FDA Device2026-08-26
FDA Recall: Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF:L2KSY2(D)/10471981 IVD, RxOnly
Siemens Healthcare Diagnostics Products Ltd.

Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.

FDA Device2026-08-26
FDA Recall: Innercool Coolblue Console, Model STx; Thermal regulating system.
Gentherm Medical, LLC

Overheating of the 115V CPU board may cause the device to shut down.

FDA Drug2026-08-26
FDA Recall: Carbamazepine Tablets, USP, 200mg, packaged in a)1000-count bottles (NDC 51407-215-10), b) 100-count
Golden State Medical Supply Inc.

CGMP deviations: tablets with black specks.

FDA Food2026-08-26
FDA Recall: Jaime’s Spanish Village: Jalapeno Ranch Dressing
Jaime’s Spanish Village

contains undeclared eggs

FDA Food2026-08-26
FDA Recall: Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz
Prospector Popcorn, LLC

Inaccurately declared nutrients including Potassium (overstated) and Calcium (overstated).

FDA Device2026-08-26
FDA Recall: MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;
Medtronic MiniMed, Inc.

Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.

FDA Food2026-08-26
FDA Recall: Whole Foods Medium Pico de Gallo Guacamole Dip, Keep Refrigerated. Packed in various sized clear pl
WFM Purchasing, LP

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

FDA Food2026-08-26
FDA Recall: Gifford's HomeMaine ice cream brand POWER PLAY FUDGE; ONE QUART (946 mL); UPC: 8 60864 00030 7
Gifford's Dairy, Inc.

Potential foreign object contamination: rubber pieces

FDA Food2026-08-26
FDA Recall: Whole Foods Spicy Guacamole Dip No Tomatoes, Keep Refrigerated. Packed in various sized clear plast
WFM Purchasing, LP

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

FDA Food2026-08-26
FDA Recall: Whole Foods Mild Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers
WFM Purchasing, LP

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

FDA Food2026-08-26
FDA Recall: Get Fresh Produce Jalapeno Peppers. Item 01896 - 2 lb. box; Item 01894 - 10 lb. box
GET FRESH PRODUCE

Potential Salmonella contamination

FDA Food2026-08-26
FDA Recall: Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging. Packaged in assorted bu
Coast Citrus Distributors

Potential Salmonella Javiana contamination

FDA Food2026-08-26
FDA Recall: Whole Foods Roasted Corn Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic co
WFM Purchasing, LP

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

FDA Drug2026-08-26
FDA Recall: ACETYLCYSTEINE SOLUTION, USP, 20% (200 mg/mL), packaged in a) 4 mL Vial NOT FOR INJECTION (NDC 0517-
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Drug2026-08-26
FDA Recall: PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL (10 mg/mL), Single-dose vial, Rx only, Manufacture
Shilpa Medicare Limited

Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials

NHTSA2026-08-2667,146 units
Rearview Camera Image May Not Display/FMVSS 111
Mitsubishi Motors North America, Inc.

A rearview image that does not display properly reduces the driver's view behind the vehicle, increasing the risk of a crash.

FDA Drug2026-08-26
FDA Recall: Atropine Sulfate injection, USP, 1 mg/mL, For intravenous Use, Sterile, packaged in a) 1 mL Single-D
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Drug2026-08-26
FDA Recall: Libtayo (cemiplimab-rwlc) Injection, 350 mg/7 mL (50 mg/mL), For Intravenous Infusion After Dilution
Regeneron Pharmaceuticals Inc

Lack of Assurance of Sterility

NHTSA2026-08-26106 units
Lower Control Arm May Damage Subframe
Rennline Automotive

A damaged subframe my lead to a loss of steering control, increasing the risk of a crash.

FDA Drug2026-08-26
FDA Recall: Acamprosate Calcium, Delayed-Release Tablets, 333 mg, 180 tablets bottles, Rx only, Mylan Pharmaceut
Mylan Pharmaceuticals Inc

Failed Dissolution Specifications

FDA Drug2026-08-26
FDA Recall: PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured
Shilpa Medicare Limited

Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials

FDA Drug2026-08-26
FDA Recall: AMINAOCAPROIC ACID INJECTION, USP, 250 mg/mL (5 g/20 mL), packaged in a) 20 mL MULTIPLE DOSE VIAL FO
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Device2026-08-26
FDA Recall: One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.
Intersurgical Inc

Devices could potentially be occluded or partially occluded.

FDA Food2026-08-26
FDA Recall: Whole Foods Spicy Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic container
WFM Purchasing, LP

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

NHTSA2026-08-26148,663 units
Wiring Harness Ground Connection Failure/FMVSS 104, 108
Ford Motor Company

A loss of driver power increases the risk of a crash. In addition, a loss of headlight function or windshield washing system function can reduce visibility, increasing the risk of a crash.

FDA Drug2026-08-26
FDA Recall: Carbamazepine Tablets, USP, 200mg, 1000 count bottles, Rx only, Manufactured by: Taro Pharmaceutical
SUN PHARMACEUTICAL INDUSTRIES INC

CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing

FDA Device2026-08-26
FDA Recall: One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device.
Intersurgical Inc

Devices could potentially be occluded or partially occluded.

FDA Device2026-08-26
FDA Recall: Beckman Coulter, Emit 2000 Quinidine Assay REF: OSR4Q229 Contents: R1: 2 x 23 mL;R2 2x13 mL
Siemens Healthcare Diagnostics, Inc.

Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine measurements, creating risk of sub-optimal patient treatment, including potential life-threatening cardiac arrhythmias or inadequate antimalarial therapy.

FDA Device2026-08-26
FDA Recall: Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplat
restor3d Inc.

Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.

FDA Device2026-08-26
FDA Recall: TD Navio Midi Speech Generating Device Model/Catalog Number: 1000798
Tobii Dynavox Llc

Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. This may cause localized heating and gas venting within the device enclosure.

FDA Device2026-08-26
FDA Recall: Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalo
Kico Knee Innovation Company

Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing

FDA Device2026-08-26
FDA Recall: American Contract Systems medical procedure kits and trays labeled as: 1) CRANI PACK - 208400, Mo
American Contract Systems Inc

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.

FDA Device2026-08-26
FDA Recall: Cardiac Workstation 5000. Product Number: 860439.
Philips North America Llc

Device will intermittently provide inaccurate data related to native heart rate.

FDA Device2026-08-26
FDA Recall: Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL, 1x14mL
Siemens Healthcare Diagnostics, Inc.

Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine measurements, creating risk of sub-optimal patient treatment, including potential life-threatening cardiac arrhythmias or inadequate antimalarial therapy.

FDA Device2026-08-26
FDA Recall: Suture Cinch Long 1pk. Endoscopic tissue approximation device.
Boston Scientific Corporation

Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.

FDA Device2026-08-26
FDA Recall: Custom Made Device Implant 6123 Navicular Cage Small Right Rev A, Model/Catalog Number 6123S R; foot
Paragon 28, Inc.

Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.

FDA Device2026-08-26
FDA Recall: EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHE
Covidien, LLC

The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.

FDA Food2026-08-26
FDA Recall: Whole Foods Mild Guacamole Dip No Tomatoes, Keep Refrigerated. Packed in various sized clear plasti
WFM Purchasing, LP

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

FDA Device2026-08-26
FDA Recall: Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703, 423704, 423705, 423707, 42370
ConvaTec, Inc

Urostomy Pouches may leak from cap during use.

FDA Device2026-08-26
FDA Recall: Lago X
Spectral Instruments Inc

Momentary absence of On-Screen "X-Ray On" banner during run readiness check.

FDA Device2026-08-26
FDA Recall: MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
Medtronic MiniMed, Inc.

Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.

FDA Device2026-08-26
FDA Recall: BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm
Bard Access Systems, Inc.

After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove obturator, due to it locking to the needle hub, due to out-of-tolerance dimensions and IFU unclarity, which may result in new needle placement, which may result in delayed therapy

FDA Device2026-08-26
FDA Recall: Beckman Coulter DxC 500 AU Clinical Analyzer Modules using software version 1.5 or lower: 1) AU w
Beckman Coulter Inc.

a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by the user, upon import of a new Parameter Package version. As a result, usercustomized calculated test rules revert silently to their default expressions, potentially generating erroneous patient test results without an explicit error notification. The issue affects instruments running software version 1.5 or lower and only occurs when a new Parameter Package is imported to a system that already has an existing Parameter Package onboard; new installations are not affected.

FDA Food2026-08-26
FDA Recall: Organic Whole Mixed Berries, Net Wt. 10 oz (284 g) plastic bags, packed in 8 bags per case of 10 oz
Publix Super Markets, Inc.

Due to potential E. coli O145:H28 contamination

FDA Device2026-08-26
FDA Recall: Beckman Coulter DxC 500i Clinical Analyzer Modules using software version 1.5 or lower: 1) DxC 50
Beckman Coulter Inc.

a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by the user, upon import of a new Parameter Package version. As a result, usercustomized calculated test rules revert silently to their default expressions, potentially generating erroneous patient test results without an explicit error notification. The issue affects instruments running software version 1.5 or lower and only occurs when a new Parameter Package is imported to a system that already has an existing Parameter Package onboard; new installations are not affected.

FDA Drug2026-08-26
FDA Recall: Cyanocobalamin injection USP, 10,000 mcg/10 mL (1,000 mcg/mL), For IM or SC Use Only, packaged in a)
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Device2026-08-26
FDA Recall: TD Navio Maxi Speech Generating Device Model/Catalog Number: 1000799
Tobii Dynavox Llc

Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. This may cause localized heating and gas venting within the device enclosure.

FDA Device2026-08-26
FDA Recall: Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525, 21-253528, 21-253530, 21-253533, 21-
Arrowhead DE LLC

Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection.

FDA Device2026-08-26
FDA Recall: Dentsply Sirona Capsule Mixer Model No. 5546068
SDI Limited

Potential for electrical discharge from unit when unplugged.

FDA Food2026-08-26
FDA Recall: Whole Foods Mango Pineapple Salsa sold as a condiment in Caribbean Mango Pineapple Turkey Burger. K
WFM Purchasing, LP

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

FDA Device2026-08-26
FDA Recall: Blanketrol II Model 222S; Thermal regulating system.
Gentherm Medical, LLC

Overheating of the 115V CPU board may cause the device to shut down.

FDA Food2026-08-26
FDA Recall: Organic Whole Blueberries, Net Wt. 48 oz (3Lb) plastic bag, packed in 6 bags per case of 10 oz each.
Publix Super Markets, Inc.

Due to potential E. coli O145:H28 contamination

FDA Food2026-08-26
FDA Recall: Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.
Prospector Popcorn, LLC

Inaccurately declared nutrients including Potassium (overstated), Calcium (overstated), and Iron (understated).

FDA Food2026-08-26
FDA Recall: Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each.
Publix Super Markets, Inc.

Due to potential E. coli O145:H28 contamination

FDA Food2026-08-26
FDA Recall: Whole Foods Trio Dip, Contains Pico de Gallo, Guacamole, Salsa. Keep Refrigerated. Packed in vario
WFM Purchasing, LP

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

FDA Device2026-08-26
FDA Recall: Cardiac Workstation 7000. Product Number: 860441.
Philips North America Llc

Device will intermittently provide inaccurate data related to native heart rate.

FDA Food2026-08-26
FDA Recall: Jaime’s Spanish Village: Jalapeno Ranch Dressing
Jaime’s Spanish Village

contains undeclared eggs

FDA Device2026-08-26
FDA Recall: Hamilton Microlab STAR Liquid Handler; Protocol Configuration Tool (PCT) v2.0.0. Used to conduct F1C
Foundation Medicine, Inc.

Software issue that can cause an increase in spontaneous software closures.

FDA Food2026-08-26
FDA Recall: Whole Foods Salsa, Heirloom Tomato. Keep Refrigerated. Packed in various sized clear plastic conta
WFM Purchasing, LP

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

FDA Device2026-08-26
FDA Recall: Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF(s):L2kSY2/10489085; L2KSY6/1048
Siemens Healthcare Diagnostics Products Ltd.

Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.

FDA Drug2026-08-26
FDA Recall: Baxter: 0.9% Sodium Chloride Injection, USP, 500 mL VIAFLEX Plastic Container
Baxter

Potential presence of particulate matter identified as fiberglass in the solution.

FDA Device2026-08-26
FDA Recall: Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus, Material Number SR-250-NPS; Per
Boston Scientific Corporation

Potential for arterial sheath tip separation or partial tip separation during use.

FDA Food2026-08-26
FDA Recall: Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz.
Prospector Popcorn, LLC

Inaccurately declared nutrients including Carbohydrates (understated) and Cholesterol (understated).

FDA Device2026-08-26
FDA Recall: Blanketrol III, Model 233; Thermal regulating system.
Gentherm Medical, LLC

Overheating of the 115V CPU board may cause the device to shut down.

FDA Drug2026-08-26
FDA Recall: Nitroglycerin injection, USP, 50 mg/10 mL (5 mg/mL), packaged in a) 10 mL vials (NDC 0517-4810-01),
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Drug2026-08-26
FDA Recall: Selenious Acid Injection, USP 12 mcg/2 mL (6 mcg/2mL), For intravenous use, packaged in a) 2mL Singl
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Drug2026-08-26
FDA Recall: Tralement (trace elements injection 4*, USP), packaged in a) 1mL Single Dose vials (NDC 0517-9305-01
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Device2026-08-26
FDA Recall: OverStitch Suture Cinch, 1pk. Endoscopic tissue approximation device.
Boston Scientific Corporation

Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.

FDA Drug2026-08-26
FDA Recall: Multrys (Trace Elements Injection 4, USP), For intravenous infusion, packaged in a) 1 mL Single-Dose
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Device2026-08-26
FDA Recall: Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001
Paragonix Technologies Inc.

Due to a firmware defect, the portable organ transfer device datalogger may lose its configuration, resulting in a blank screen and loss of displayed preservation parameters.

FDA Drug2026-08-26
FDA Recall: niCARdipine Hydrochloride Injection, USP, 25 mg/10mL (2.5 mg/mL), packaged in a) 10 mL Single Dose V
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Device2026-08-26
FDA Recall: Boston Scientific ENROUTE Transcarotid Neuroprotection System, Material Number SR-200-NPS; Percutan
Boston Scientific Corporation

Potential for arterial sheath tip separation or partial tip separation during use.

FDA Drug2026-08-26
FDA Recall: Cyanocobalamin injection USP, 1,000 mcg/mL, For IM or SC Use Only, packaged in a) 1 mL Multi-Dose Vi
American Regent, Inc.

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

FDA Device2026-08-26
FDA Recall: Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A, Model/Catalog Number 6123N R; fo
Paragon 28, Inc.

Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.

FDA Device2026-08-26
FDA Recall: Ami HTX
Spectral Instruments Inc

Momentary absence of On-Screen "X-Ray On" banner during run readiness check.

FDA Device2026-08-26
FDA Recall: Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131
Fort Defiance Industries, LLC

The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which could result in an unreliable fault current return path.

FDA Device2026-08-26
FDA Recall: GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous v
Maquet Critical Care AB

The module did not undergo electrical safety tests and functional tests during production.

FDA Drug2026-08-25
FDA Recall: Baxter: Anticoagulant Sodium Citrate Solution USP, 250 mL VIAFLEX Plastic Container
Baxter

Potential presence of particulate matter identified as fiberglass in the solution

FDA Drug2026-08-25
FDA Recall: Baxter: 70% Dextrose Injection, USP in 2000 mL VIAFLEX Plastic Container
Baxter

Potential presence of particulate matter identified as stainless steel particles in the solution.

NHTSA2026-08-2560 units
Insufficient Joint Strength and Missing Seat Belt Anchor/FMVSS 210, 221
Daimler Trucks North America, LLC

A seat belt anchor with a missing connector plate may fail to properly restrain the driver and insufficient joint strength may not adequately protect passengers, increasing the risk of injury in a crash.

FDA Food2026-08-24
FDA Recall: Donutful: Chocolate Dipped Vanilla Cake Donuts
Donutful

Undeclared milk allergen

FDA Food2026-08-24
FDA Recall: Momchipz: Veggie Chips Broccoli Florets & Cauliflower
Momchipz

undeclared wheat

NHTSA2026-08-2421,290 units
Occupant Detection System May Fail to Suppress Air Bag/FMVSS 208
Kia America, Inc.

A child in the front seat may be at a greater risk of injury if the air bag deploys during a crash.

NHTSA2026-08-24130 units
Trailer Tongue May Crack
Cornell Pump Company LLC

Instability while towing increases the risk of a crash.

FDA Drug2026-08-24
FDA Recall: Vitruvias Therapeutics: Thyroid Tablets, USP 30 mg
Vitruvias Therapeutics

Potential for the Product to be Superpotent

NHTSA2026-08-24811 units
Seat Ventilation Harness Can Cause Short Circuit
PACCAR Incorporated

A short circuit increases the risk of a fire.