Safety Recalls

17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 3,201–3,250 of 17,559

• Medical Device Recall · March 5, 2026

  Cook Incorporated

  COOK MEDICAL Blue Rhino¿ G2-Multi Percutaneous Tracheostomy Introducer Tray: Reference Part Number C-PTISY-100-HC-G-NA, Order Number G57703; Reference Part Number C-PTISY-100-UNL-HC-G-NA, Order Num

  Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

  Class II

• Medical Device Recall · March 5, 2026

  Cook Incorporated

  COOK MEDICAL Approach CTO-18 Micro Wire Guide, Reference Part Number CMW-14-190-18G, Order Number G50788; Reference Part Number CMW-14-300-18G, Order Number G50792

  Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

  Class II

• Medical Device Recall · March 4, 2026

  Koven Technology, Inc.

  Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe Model/Catalog Number: ES-100V3 (device); BT2M20S8C (2 MHz fetal probe). Software Version: N/A Product

  Product labeling includes a fetal indication for use that is not cleared under its 510(k).

  Class II

• Food Recall · March 4, 2026

  Disaronno Ingredients S.p.a.

  Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag, packed 8 bags per master case of 2 Kg (4.41 lb) each total case weight,16 Kg / 35.27 lb

  Undeclared allergen Milk. The presence of the milk allergen in the product was found to exceed acceptable levels despite the product being labeled with the statement *May contain milk. *

  Class II

• Medical Device Recall · March 3, 2026

  Oxoid Australia Pty Limited

  OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem

  Oxoid 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

• Drug Recall · March 3, 2026

  Rising Pharma Holding, Inc.

  Product label: Temozolomide Capsules, 5mg, packaged in 5-capsule bottles, Rx only, Manufactured for: Rising Pharmaceuticals, Inc., Allendale, NJ 07401, Country of origin: Taiwan, NDC 16571-816-51.

  Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-month long term stability testing

  Class II

• Medical Device Recall · March 3, 2026

  Angiodynamics, Inc.

  Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.: 10714014; Product/UPN No.: H787107140145 (Box), H787107140140 (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

• Drug Recall · March 3, 2026

  K.C. Pharmaceuticals, Inc

  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.PerrigoD

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · March 3, 2026

  Angiodynamics, Inc.

  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: 5

  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 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 ar

  Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.

  Class II

• Drug Recall · March 3, 2026

  K.C. Pharmaceuticals, Inc

  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) Good

  Lack of Assurance of Sterility

  Class II

• Vehicle Recall · March 3, 2026

  Ford Motor Company

  2026 FORD F-350 SD

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

  Unclassified

• Vehicle Recall · March 3, 2026

  Ford Motor Company

  2026 FORD E-450

  A backup alarm that fails to alert pedestrians and other vehicles of a reversing vehicle, increases the risk of crash or injury.

  Unclassified

• 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 flexible

  Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.

  Class II

• Drug Recall · March 3, 2026

  Owen Biosciences Inc.

  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 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

• Drug Recall · March 3, 2026

  K.C. Pharmaceuticals, Inc

  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, IL

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · March 3, 2026

  Angiodynamics, Inc.

  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

  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.

  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

• Medical Device Recall · March 3, 2026

  Angiodynamics, Inc.

  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

  Angiodynamics, Inc.

  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 p

  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

• Drug Recall · March 3, 2026

  Owen Biosciences Inc.

  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 McKinn

  Chemical contamination: Presence of benzene

  Class II

• Medical Device Recall · March 3, 2026

  Angiodynamics, Inc.

  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 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

  Angiodynamics, Inc.

  AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers; ACCU-VU PT 4F X 70CM 035 NB 10SH 21 R/O 1CM; Catalog No.: 13709804; Product/UPN No.: H787137098045 (Box), H787137098040 (Pou

  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 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 i

  Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.

  Class II

• Medical Device Recall · March 3, 2026

  Angiodynamics, Inc.

  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

  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.

  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.

  Class II

• Medical Device Recall · March 3, 2026

  Wilson-Cook Medical Inc.

  Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

  Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.

  Class II

• Medical Device Recall · March 3, 2026

  Angiodynamics, Inc.

  Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB 0SH; Catalog No.: 10714016; Product/UPN No.: H787107140165 (Box), H787107140160 (Pouch); Box Quantity: 5 pouch

  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

  Angiodynamics, Inc.

  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 pouche

  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

• Vehicle Recall · March 3, 2026

  Ford Motor Company

  2023 FORD BRONCO, 2023 FORD EDGE, 2024 FORD EDGE, 2024 FORD BRONCO

  A rearview camera that fails to display an image can reduce the driver’s view behind the vehicle, increasing the risk of a crash.

  Unclassified

• 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 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

• 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 FD10F; System Code: 722002;

  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

  Angiodynamics, Inc.

  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 (P

  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

  Angiodynamics, Inc.

  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 pouche

  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; System Code: (1) 722006, (2)722012, (3)722028;

  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

  Angiodynamics, Inc.

  Soft-Vu Angiographic Catheter, Sos Omni Selective (1), Non-Braided; SOFT-VU SO1 4F X 80CM 038 NB 0SH; Catalog No.: 10714024; Product/UPN No.: H787107140245 (Box), H787107140240 (Pouch); Box Quanti

  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 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.

  Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (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

  Angiodynamics, Inc.

  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

• Vehicle Recall · March 3, 2026

  Ford Motor Company

  2023 FORD EXPLORER, 2023 LINCOLN AVIATOR, 2024 FORD EXPLORER, 2024 LINCOLN AVIATOR

  An incorrectly displayed rearview image can reduce the driver’s view behind the vehicle, increasing the risk of a crash.

  Unclassified

• 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

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;

  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

  Angiodynamics, Inc.

  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 pouche

  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

  Angiodynamics, Inc.

  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

• Vehicle Recall · March 3, 2026

  Ford Motor Company

  2025 FORD EXPLORER

  A headlight that turns incorrectly can result in increased glare to other road users, increasing the risk of a crash.

  Unclassified