Safety Recalls
RSS ↗17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,251–3,300 of 17,559
- Unclassified
Vehicle Recall · March 3, 2026
2025 FORD EXPLORER, 2025 FORD MUSTANG, 2025 LINCOLN NAUTILUSAn unexpected loss of drive power increases the risk of a crash.
- 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
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (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
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
Food Recall · March 3, 2026
Ajinomoto Foods North America Inc.
Item 81153 Kroger Chinese Inspiration Vegetable Fried Rice - Blend of long grain rice assorted vegetables & egg. Net wt. 22oz. Retail box UPC 011110041623. Product packaging is flexible bags in a masForeign 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 FD20/10; 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
Medical Device Recall · March 3, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;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 FD10/10; System Code: (1) 722005, (2)722011, (3)722027;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 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
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
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/15 OR Table; System Code: 722059;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
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
Food Recall · March 3, 2026
Ajinomoto Foods North America Inc.
Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed. SKU #097908. Net wt. 1lb. per bag. Retail bag UPC 00979085. Product packaging is flexible bags in a masterForeign 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
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
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
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
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
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
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
Drug Recall · March 3, 2026
HydroPeptide CLEAR ALLIANCE SERUM, 2.5% BENZOYL PEROXIDE, a)1 FL OZ/30ml; b) 2 FL OZ/60ml spray bottle; DIST BY HYDROPEPTIDE LLC, ISSAQUAH, WA 98027Chemical contamination: Presence of benzene
- Class II
Medical Device Recall · March 3, 2026
AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 2 R/O 2CM; Catalog No.: 13709005; Product/UPN No.: H787137090055 (Box), H787137090050 (PouThe 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 5650883 Ajinomoto Teppanyaki Style Vegetable Fried Rice - Japanese-style fried rice made with colorful vegetables in an aromatic garlic butter sauce. There are 6/9oz. bags per box or 54oz per boxForeign objects are glass varying in size from 1-3cm long and 2-4mm wide.
- Class I
- Class II
Food Recall · March 3, 2026
Ajinomoto Foods North America Inc.
Item 5650893 Ajinomoto Japanese-Style Vegetable Fried Rice made with hijiki seaweed, fried tofu, edamame, and other colorful vegetables in an umami dashi sauce Net wt. 17oz. Retail box UPC 07175750893Foreign 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, 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
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 6430153 Ajinomoto Vegetable Gyoza Dumplings. Net wt. 24.7oz. per bag. Retail box UPC: 071757010109. Product packaging is flexible bags in a master case or flexible bags in cartons in a master caForeign objects are glass varying in size from 1-3cm long and 2-4mm wide.
- Class II
Medical Device Recall · March 2, 2026
Civco Medical Instruments Co. Inc.
eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
- Class I
Medical Device Recall · March 2, 2026
Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
- Class I
Medical Device Recall · March 2, 2026
Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- Class I
Medical Device Recall · March 2, 2026
Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- Class II
Medical Device Recall · March 2, 2026
Civco Medical Instruments Co. Inc.
eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
- Class II
Medical Device Recall · March 2, 2026
Civco Medical Instruments Co. Inc.
eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
- Class I
Drug Recall · March 2, 2026
Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive, Waukegan, IL 60085.Non-Sterility: microbial contamination identified as Paenibacillus phoenicis
- Class II
Food Recall · March 2, 2026
Secondary Packaging: ZHONG HUA CHAO MIAN NOODLE INGREDIENTS: ENRICHED FLOUR, WATER, STARCH, SALT, POTASSIUM, CARBONATE AND BENZOATE OF SODA ADDED AS PRESERVATIVE F.D. & C. YELLOW COLOR #5 & #5 (TARTRAUndeclared wheat and Yellow #6.
- Class II
Medical Device Recall · March 2, 2026
Civco Medical Instruments Co. Inc.
eTRAX Needle System Starter Kit 16G(for Aurora Trackers), Part Number 667-151There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
- Class II
Drug Recall · March 2, 2026
Children's Ibuprofen Oral Suspension, USP, 100 mg per 5mL, 4 FL OZ (120 mL) bottle, Manufactured for: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, Made in India, NDC 51672-5321-8.Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.
- Class I
Medical Device Recall · March 2, 2026
Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
- Class II
Medical Device Recall · March 2, 2026
Civco Medical Instruments Co. Inc.
eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
- Class I
Medical Device Recall · March 2, 2026
Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- Class I
Medical Device Recall · March 2, 2026
Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
- Class II
Medical Device Recall · March 2, 2026
Civco Medical Instruments Co. Inc.
eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
- Class I
Medical Device Recall · March 2, 2026
Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- Class I
Medical Device Recall · March 2, 2026
Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
- Class II
Medical Device Recall · March 2, 2026
Civco Medical Instruments Co. Inc.
eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
- Class II
Medical Device Recall · March 2, 2026
Civco Medical Instruments Co. Inc.
eTRAX Needle System Starter Kit 14G (for Aurora Trackers), Part Number 667-150There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
- Class II
Medical Device Recall · February 27, 2026
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO DRAPE PACK (ADLUG)642-LF DYNJ47665D ANGIO PACK DYNJ30565D ANGIOGRAPHY PACK-LF DYNJ0854485VFirm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.