Safety Recalls

15,184 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 1,751–1,800 of 15,184

• 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, 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

• Drug Recall · March 3, 2026

  Owen Biosciences Inc.

  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 98027

  Chemical contamination: Presence of benzene

  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

• 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

  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

  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

  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 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, 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

  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

• 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

  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

• Food Recall · March 3, 2026

  FRITO-LAY NORTH AMERICA, INC.

  Miss Vickies Spicy Dill Pickle; 8 oz bag

  Undeclared Allergen: Milk

  Class I

• 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 07175750893

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

  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.

  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 (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

• 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

• 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 master

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

  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 ca

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

  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 mas

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

  Class II

• Medical Device Recall · March 2, 2026

  Philips Respironics, Inc.

  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 I

• Medical Device Recall · March 2, 2026

  Civco Medical Instruments Co. Inc.

  eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158

  There 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

  Philips Respironics, Inc.

  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, Inc.

  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

  Civco Medical Instruments Co. Inc.

  eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159

  There 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 16G(for Aurora Trackers), Part Number 667-151

  There 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 12G (for Aurora Trackers), Part Number 667-149

  There 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 - 14G(for Aurora Trackers), Part Number 667-157

  There 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

  Philips Respironics, Inc.

  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

  Civco Medical Instruments Co. Inc.

  eTRAX Needle System Starter Kit 14G (for Aurora Trackers), Part Number 667-150

  There 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

  Philips Respironics, Inc.

  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 I

• Drug Recall · March 2, 2026

  Cardinal Health 200, LLC

  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 I

• Food Recall · March 2, 2026

  CNC Noodle Corporation

  Secondary Packaging: STEAM NOODLES INGREDIENTS: ENRICHED FLOUR, WATER, STARCH, SALT, POTASSIUM, CARBONATE AND BENZOATE OF SODA ADDED AS PRESERVATIVEM F.D. & C. YELLOW COLOR #5 & #6 (TARTRAZINE) ARTIFI

  Undeclared wheat.

  Class II

• Medical Device Recall · March 2, 2026

  Civco Medical Instruments Co. Inc.

  eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

  There 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 18G (for Aurora Trackers), Part Number 667-152

  There 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

  Philips Respironics, Inc.

  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 I

• Medical Device Recall · March 2, 2026

  Philips Respironics, Inc.

  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 I

• Drug Recall · March 2, 2026

  STRIDES PHARMA INC

  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 II

• Food Recall · March 2, 2026

  CNC Noodle Corporation

  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 (TARTRA

  Undeclared wheat and Yellow #6.

  Class II

• Medical Device Recall · March 2, 2026

  Philips Respironics, Inc.

  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 · February 27, 2026

  Medline Industries, LP

  Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. HEAD AND NECK CDS-LF, Medline SKU # CDS780138K;

  Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

  Class I

• Medical Device Recall · February 27, 2026

  Medline Industries, LP

  Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BASIC CL PACK-LF DYN

  Unapproved design changes to the products outside of the 510(k) clearance.

  Class II

• Medical Device Recall · February 27, 2026

  Medline Industries, LP

  Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ANGIO KIT PACK DYNJ50783B ANGIO PHC DYNJ37485C C.I.C.N. ANGIO PACK DYNJ53064B FHT P NEURO PACK DY

  Unapproved design changes to the products outside of the 510(k) clearance.

  Class II

• Medical Device Recall · February 27, 2026

  Medline Industries, LP

  Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. ROBOTIC PACK, Medline SKU # DYNJ58475F; 2. URO/G

  Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

  Class I

• Medical Device Recall · February 27, 2026

  Medline Industries, LP

  Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes MINOR ENT SINUS PACK-LF DYNJ0101278F DYNJ0101278G DYNJ0101278I SINUS PACK DYNJ56262

  Unapproved design changes to the products outside of the 510(k) clearance.

  Class II

• Medical Device Recall · February 27, 2026

  Medline Industries, LP

  Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BIOPSY PACK DYNJ38587A, DYNJ38587B BIOPSY/DRAINAGE TRAY-LF DYNJ30078D W LINQ PACK DYNJ59108B

  Unapproved design changes to the products outside of the 510(k) clearance.

  Class II

• Medical Device Recall · February 27, 2026

  Spacelabs Healthcare, Inc.

  Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor

  Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve error with no CO measurement or Irregular Curve error with CO measurement not automatically excluded, which may result in inaccurate readings, or the need of additional readings, which may lead to delayed care and/or fluid overload.

  Class II

• Medical Device Recall · February 27, 2026

  Medline Industries, LP

  Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BARIATRIC DYNJ905153M, DYNJ905153N GENERAL LAPAROSCOPY PACK DYNJ81602 LAPAROSCOPY DYNJ905157K, DYNJ9

  Unapproved design changes to the products outside of the 510(k) clearance.

  Class II

• Medical Device Recall · February 27, 2026

  Cardinal Health 200, LLC

  Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777

  The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within the packages are U-100 Insulin syringes.

  Class II