Safety Recalls
RSS ↗15,184 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 1,701–1,750 of 15,184
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/20 OR Table; System Code: 722039;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Unclassified
Vehicle Recall · March 3, 2026
2026 FORD E-450A backup alarm that fails to alert pedestrians and other vehicles of a reversing vehicle, increases the risk of crash or injury.
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Straight Art, Non-Braided; SOFT-VU STR ART 4F X 65CM 035 NB 0SH; Catalog No.: 10731401; Product/UPN No.: H787107314015 (Box), H787107314010 (Pouch); Box Quantity: 5The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Drug Recall · March 3, 2026
Dry Eye Relief Eye Drops, (glycerin 0.2%, hypromellose 0.2% and polyethylene glycol 400 1%) 0.5 FL OZ (15 mL) bottles; a) GERI CARE, Distributed by: Gericare Pharmaceuticals Corp., Lakewood, NJ 08701Lack of Assurance of Sterility
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 038 NB 0SH; Catalog No.: 10714017; Product/UPN No.: H787107140175 (Box), H787107140170 (Pouch); Box Quantity: 5 poucheThe affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 NB 0SH; Catalog No.: 10714021; Product/UPN No.: H787107140215 (Box), H787107140210 (Pouch); Box Quantity: 5 pouches;The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Food Recall · March 3, 2026
Ajinomoto Foods North America Inc.
Item 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice Savory Vegetable - A Chinese Style Fried Rice with Edamame, Carrots, Fire Roasted Corn & Red Bell Peppers Prepared with Sweet Soy Sauce InfusForeign objects are glass varying in size from 1-3cm long and 2-4mm wide.
- Class II
Medical Device Recall · March 3, 2026
AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10 R/O 6@1CM 4@5CM; Catalog No.: 13709604; Product/UPN No.: H787137096045 (Box),The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Food Recall · March 3, 2026
Ajinomoto Foods North America Inc.
Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp, vegetables & fried rice with oyster flavored sauce. Net wt. 48oz or 3lbs. per box. Retail box UPC 070077811465. Product packaging is flexibleForeign objects are glass varying in size from 1-3cm long and 2-4mm wide.
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 035 NB 6SH; Catalog No.: 10732301; Product/UPN No.: H787107323015 (Box), H787107323010 (Pouch); Box Quantity: 10 units;The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 65CM 038 NB 10SH; Catalog No.: 10714002; Product/UPN No.: H787107140025 (Box), H787107140020 (Pouch); Box Quantity: 10 pouches;The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Food Recall · March 3, 2026
Ajinomoto Foods North America Inc.
Item 5650233 Trader Joe's Vegetable Fried Rice, net wt. 1lb per bag. Retail bag UPC 00521482. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There aForeign objects are glass varying in size from 1-3cm long and 2-4mm wide.
- Class II
Medical Device Recall · March 3, 2026
OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystemOxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to inconclusive result from ambiguous color reactions in wells.
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/15; System Code: 722058;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Drug Recall · March 3, 2026
SLMD BP Acne Spot Treatment, 10% Benzoyl Peroxide, 0.5 fl. oz - 15 mL bottles, Sandra Lee MD, Distributed by Skin PS Brands, Culver City, CA90232.Chemical contamination: Presence of benzene
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 5 M12; System Code: (1)722227, (2)722231;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 65CM 038 NB 0SH; Catalog No.: 10714011; Product/UPN No.: H787107140115 (Box), H787107140110 (Pouch); Box Quantity: 5 pouchesThe affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Drug Recall · March 3, 2026
FHF Farmhouse Fresh, Midnight Clearing, NIGHT LOTION, 2.5% BENZOYL PEROXIDE ACNE TREATMENT, OTC a) 0.5 fl. oz./15ml; and b)1 fl. oz./30ml tubes; Made in the USA for FarmHouse Fresh, 8797 CR 858 McKinnChemical contamination: Presence of benzene
- Class II
Food Recall · March 3, 2026
Ajinomoto Foods North America Inc.
Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per package. Retail package UPC: 071757055483. Product packaging is flexible bags in a master case or flexible bags in cartons iForeign objects are glass varying in size from 1-3cm long and 2-4mm wide.
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/20; System Code: 722038;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Food Recall · March 3, 2026
Ajinomoto Foods North America Inc.
Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12ct. Retail bag UPC: None. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There arForeign objects are glass varying in size from 1-3cm long and 2-4mm wide.
- Class II
Drug Recall · March 3, 2026
Artificial Tears Sterile Lubricant Eye Drops (polyvinyl alcohol 0.5%, povidone 0.6%), 0.5 FL OZ (15 mL) bottles; a) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.com, NDC 70Lack of Assurance of Sterility
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB 0SH; Catalog No.: 10734301; Product/UPN No.: H787107343015 (Box), H787107343010 (Pouch); Box Quantity: 5 pouches;The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/10; System Code: 722029;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Drug Recall · March 3, 2026
Ultra Lubricating Eye Drops (polyethylene 400 0.4%, propylene glycol 0.3%), Sterile, 0.5 FL OZ (15mL) bottles; a) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.com, NDC 7000Lack of Assurance of Sterility
- Class II
Drug Recall · March 3, 2026
Sterile Eye Drops ORIGINAL FORMULA (tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15mL) bottles; a) Good Sense Sterile Eye Drops, Distributed By: Perrigo Direct, Inc., Peachtree City, GA 30269, www.PerrigoDLack of Assurance of Sterility
- Class II
Medical Device Recall · March 3, 2026
Soft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 NB 0SH; Catalog No.: 10710013; Product/UPN No.: H787107100135 (Box), H787107100130 (Pouch); Box Quantity: 5 pouches;The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 038 NB 6SH; Catalog No.: 10714001; Product/UPN No.: H787107140015 (Box), H787107140010 (Pouch); Box Quantity: 10 poucheThe affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Drug Recall · March 3, 2026
EYE DROPS Advanced Relief, (dextran 70 0.1%, polyethylene glycol 400 1% and tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15 mL) bottles, Sterile; a) Walgreens, DISTRIBUTED BY: WALGREEN CO., DEERFIELD, ILLack of Assurance of Sterility
- Class II
Drug Recall · March 3, 2026
Sterile EYE DROPS REDNESS LUBRICANT (glycerin 0.25% and naphazoline HCl 0.012%), 0.5 fl oz (15 mL) bottles; a) Industrial Eye Relief, Distributed by: Cintas Corp., Mason, OH 45040, UPC 130209; b) GoodLack of Assurance of Sterility
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Drug Recall · March 3, 2026
SLMD Benzoyl Peroxide Acne Lotion, Benzoyl Peroxide 2.5%, a) 0.7 fl. oz - 21 mL and b) 1.5 fl. oz. - 44mL bottles, SANDRA LEE MD., Distributed by Skin PS Brands, Culver City, CA 90232.Chemical contamination: Presence of benzene
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Class II
Drug Recall · March 3, 2026
Sterile EYE DROPS AC (tetrahydrozoline HCl 0.05%, zinc sulfate 0.25%), 0.5 fl. oz. (15 mL) bottles; a) Best Choice, PROUDLY DISTRIBUTED BY: VALU MERCHANDISERS, CO., 5000 KANSAS AVE, KANSAS CITY, KS 66Lack of Assurance of Sterility
- Class II
Drug Recall · March 3, 2026
STERILE EYE DROPS SOOTHING TEARS (polyethylene glycol 400 0.4% and propylene glycol 0.3%), 0.5 OZ 0.5 fl oz (15 mL) bottles; a) Rugby LUBRICATING EYE DROPS, Distributed by: Rugby Laboratories, LivoniLack of Assurance of Sterility
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 65CM 038 NB 0SH; Catalog No.: 10714009; Product/UPN No.: H787107140095 (Box), H787107140090 (Pouch); Box Quantity: 5 poucheThe affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Food Recall · March 3, 2026
Ajinomoto Foods North America Inc.
Item 5654390 Ajinomoto Golden Tiger Vegetable Fried Rice - Long grain white rice and crispy vegetables in a savory sauce. Net wt. 3lbs per bag. Retail bag UPC 076366565439. Product packaging is flexiForeign objects are glass varying in size from 1-3cm long and 2-4mm wide.
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 100CM 038 NB 0SH; Catalog No.: 10714018; Product/UPN No.: H787107140185 (Box), H787107140180 (Pouch); Box Quantity: 5 poucheThe affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Unclassified
Vehicle Recall · March 3, 2026
2023 FORD EXPLORER, 2023 LINCOLN AVIATOR, 2024 FORD EXPLORER, 2024 LINCOLN AVIATORAn incorrectly displayed rearview image can reduce the driver’s view behind the vehicle, increasing the risk of a crash.
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 100CM 035 NB 10SH; Catalog No.: 10707103; Product/UPN No.: H787107071035 (Box), H787107071030 (Pouch); Box Quantity: 10;The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Medical Device Recall · March 3, 2026
Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided; SOFT-VU HH1 4F X 100CM 038 NB 0SH; Catalog No.: 10714040; Product/UPN No.: H787107140405 (Box), H787107140400 (Pouch); Box Quantity: 5 pThe affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Class II
Medical Device Recall · March 3, 2026
AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (PThe affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Unclassified
Vehicle Recall · March 3, 2026
2023 FORD BRONCO, 2023 FORD EDGE, 2024 FORD EDGE, 2024 FORD BRONCOA rearview camera that fails to display an image can reduce the driver’s view behind the vehicle, increasing the risk of a crash.
- Class II
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10C; System Code: 722001;Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.