All Recalls

1335 recalls found

Export CSV
DateSourceProductBrandSeverityUnits
2026-05-06NHTSAContact with Drive Belt Pully May Damage and Cause Oil Lines to LeakCorp. Micro Bird, Inc.N/A902
2026-05-06FDA DeviceFDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SPNG NEURO 1X1Medline Industries, LPClass IIN/A
2026-05-06FDA DeviceFDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. ANTERIOR Medline Industries, LPClass IIN/A
2026-05-06FDA DeviceFDA Recall: Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog NumbeAdvanced Bionics, LLCClass IIN/A
2026-05-06FDA DeviceFDA Recall: Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. ModPhilips North AmericaClass IIN/A
2026-05-06FDA DeviceFDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204.DEPUY (IRELAND)Class IIN/A
2026-05-06FDA DrugFDA Recall: fentaNYL Citrate Injectable Solution, Narcotic, CII, 1250 mcg/25mL (50 mcg per mL), 25 mL, wells phaWells Pharma of Houston LLCClass IIN/A
2026-05-06FDA DrugFDA Recall: fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, WeWells Pharma of Houston LLCClass IIN/A
2026-05-06FDA DrugFDA Recall: GenTeal Tears, Lubricant Eye Gel, Sterile, 10g (0.34 Fl oz), Distributed by: Alcon Laboratories, IncAlcon Research LLCClass IIN/A
2026-05-06FDA DeviceFDA Recall: WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor, WHILL, INC.Class IN/A
2026-05-06FDA DeviceFDA Recall: WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor battWHILL, INC.Class IN/A
2026-05-06FDA DeviceFDA Recall: Brand Name: Genius" Review Station Product Name: Genius" Review Station Display (Barco Monitor) MoHologic, IncClass IIN/A
2026-05-06FDA DeviceFDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. CATARACT Medline Industries, LPClass IIN/A
2026-05-06FDA DeviceFDA Recall: Medline and Centurion medical procedure kits, containing Medline Neuro Sponges (1229 in total), HEADMedline Industries, LPClass IIN/A
2026-05-06FDA DeviceFDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. PLASTICSMedline Industries, LPClass IIN/A
2026-05-06FDA DeviceFDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. SPINE PROCEMedline Industries, LPClass IIN/A
2026-05-06FDA DeviceFDA Recall: Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.Philips North AmericaClass IIN/A
2026-05-06FDA DrugFDA Recall: Similasan, iVIZIA, Sterile Lubricant Eye Drops (Povidone 0.5%), 0.33 Fl oz (10 mL), Made in France, Thea Pharma, Inc.Class IIN/A
2026-05-06FDA FoodFDA Recall: Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; ProduHEMU TRADING INCClass IN/A
2026-05-06FDA DeviceFDA Recall: Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLYMerit Medical Systems, Inc.Class IIN/A
2026-05-06FDA FoodFDA Recall: KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, 818812022208, Ganesha EnterprisGanesha Enterprises LLCClass IIN/A
2026-05-06FDA DeviceFDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges (4077 in total), LAMINECTOMY, CRANIMedline Industries, LPClass IIN/A
2026-05-06FDA DrugFDA Recall: Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (1Water-Jel Technologies, LLCClass IIIN/A
2026-05-06FDA DeviceFDA Recall: Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for tMedtronic, Inc.Class IIN/A
2026-05-06FDA FoodFDA Recall: 52USA brand POPPING BOBA; PASSION FRUIT FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, frGuangdong Zonegoing Food Co., LTDClass IIN/A
PreviousPage 3 of 54Next