Safety Recalls

17,395 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 551–600 of 17,395

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Shilpa Medicare Limited

  PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus Lifesciences Limited, Ahmedabad, India; Distributed by: Amneal Pharmaceuticals LC, Bridgew

  Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials

  Class II

• Medical Device Recall · July 29, 2026

  Diagnostica Stago, Inc.

  STA Staclot Protein S, Model/Catalog Number: 00746-Reagent Lot number 273074; qualitative and quantitative factor deficiency test

  A positive drift in QC values within the reagent's stated 4-hour onboard stability period was identified

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Medical Device Recall · July 29, 2026

  Cardinal Health 200, LLC

  Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,ROBOTICS DH , Catalog Number: PGOCRDNHD; 2) KIT, EAS ROBOTIC , Catalog Numbe

  The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

  Class II

• Medical Device Recall · July 29, 2026

  Cardinal Health 200, LLC

  Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,MAXILLOFACIAL PRESBYTERIAN, Catalog Number: PWV2MF01D

  The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Medical Device Recall · July 29, 2026

  Cardinal Health 200, LLC

  Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, ENT HARVEST , Catalog Number: PEVMETBJX; 2) KIT, ENT HARVEST , Catalog Numbe

  The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-0

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Medical Device Recall · July 29, 2026

  Fresenius Medical Care Renal Therapies Group, LLC

  CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors; Model Number: 03-2522-1;

  Communication to recommend reviewing the IFU and ensuring that all treatment preparation and handling steps are performed as instructed.

  Class II

• Medical Device Recall · July 29, 2026

  Nova Biomedical Corporation

  StatStrip Glucose and B- Ketone meter. Model No: 63910. Glucose test system.

  A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode including patient identification (ID) barcodes and quality control (QC) solution ID barcodes when a new barcode is scanned, resulting in the prior barcode information remaining displayed on the screen for the current test. When this defect occurs and the operator accepts the incorrectly displayed patient information without recognizing the mismatch, the current patient's glucose result will be incorrectly assigned to the previous patient's medical record and transmitted to the data management system (DMS), and the current patient's medical record will not receive a result, leaving their glucose status unrecorded and their clinical management without the information needed to guide treatment decisions. The previous patient, whose medical record now contains a glucose result that does not belong to them, may receive inappropriate clinical intervention based on that erroneous result, particularly in critically ill patients, neonates, and infants who cannot communicate symptoms or self-treat. The defect also affects QC barcode scanning: if a QC scan triggers the same retention behavior, QC results may be attributed to an incorrect identifier or QC tests may fail without the user recognizing the underlying cause. This defect does not affect the analytical accuracy of glucose measurements.

  Class I

• Drug Recall · July 29, 2026

  Prestige Brands Holdings

  CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC

  Lack of assurance of sterility. The recall is due to potential contamination

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-724-04.

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-722-02

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202.NDC 71170-712-03

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-822-02

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-812-03

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Medical Device Recall · July 29, 2026

  Nova Biomedical Corporation

  StatStrip Glucose and B- Ketone meter. Model No: 63683. Glucose test system.

  A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode including patient identification (ID) barcodes and quality control (QC) solution ID barcodes when a new barcode is scanned, resulting in the prior barcode information remaining displayed on the screen for the current test. When this defect occurs and the operator accepts the incorrectly displayed patient information without recognizing the mismatch, the current patient's glucose result will be incorrectly assigned to the previous patient's medical record and transmitted to the data management system (DMS), and the current patient's medical record will not receive a result, leaving their glucose status unrecorded and their clinical management without the information needed to guide treatment decisions. The previous patient, whose medical record now contains a glucose result that does not belong to them, may receive inappropriate clinical intervention based on that erroneous result, particularly in critically ill patients, neonates, and infants who cannot communicate symptoms or self-treat. The defect also affects QC barcode scanning: if a QC scan triggers the same retention behavior, QC results may be attributed to an incorrect identifier or QC tests may fail without the user recognizing the underlying cause. This defect does not affect the analytical accuracy of glucose measurements.

  Class I

• Medical Device Recall · July 29, 2026

  Nova Biomedical Corporation

  StatStrip Glucose Hospital Meter System. Model No: 63685. Glucose test system.

  A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode including patient identification (ID) barcodes and quality control (QC) solution ID barcodes when a new barcode is scanned, resulting in the prior barcode information remaining displayed on the screen for the current test. When this defect occurs and the operator accepts the incorrectly displayed patient information without recognizing the mismatch, the current patient's glucose result will be incorrectly assigned to the previous patient's medical record and transmitted to the data management system (DMS), and the current patient's medical record will not receive a result, leaving their glucose status unrecorded and their clinical management without the information needed to guide treatment decisions. The previous patient, whose medical record now contains a glucose result that does not belong to them, may receive inappropriate clinical intervention based on that erroneous result, particularly in critically ill patients, neonates, and infants who cannot communicate symptoms or self-treat. The defect also affects QC barcode scanning: if a QC scan triggers the same retention behavior, QC results may be attributed to an incorrect identifier or QC tests may fail without the user recognizing the underlying cause. This defect does not affect the analytical accuracy of glucose measurements.

  Class I

• Food Recall · July 28, 2026

  Wonton Specialists

  Wonton Specialist Inc. Wonton Noodle, 12 oz - packaged in foam tray overwrapped with clear plastic and 5lb - packaged in clear plastic bags

  Undeclared FD&C Red No. 40

  Class III

• Medical Device Recall · July 28, 2026

  Ventec Life Systems, Inc.

  REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve

  Labeling; Oxygen Cylinders do not contain required medical gas labeling

  Class II

• Food Recall · July 28, 2026

  Wonton Specialists

  Wonton Specialist Inc. Dumpling Skin, 16 oz - packaged in foam tray overwrapped with clear plastic

  Undeclared FD&C Red No. 40

  Class III

• Drug Recall · July 28, 2026

  Regeneron Pharmaceuticals Inc

  Libtayo (cemiplimab-rwlc) Injection, 350 mg/7 mL (50 mg/mL), For Intravenous Infusion After Dilution, Single-Dose Vial, Rx only, Manufactured by: Regeneron Pharmaceuticals, Inc., Tarrytown, NY 10591;

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 28, 2026

  Ventec Life Systems, Inc.

  REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver

  Labeling; Oxygen Cylinders do not contain required medical gas labeling

  Class II

• Food Recall · July 28, 2026

  Wonton Specialists

  Wonton Specialist Inc. Wonton Skin, 16 oz - packaged in foam tray overwrapped with clear plastic

  Undeclared FD&C Red No. 40

  Class III

• Medical Device Recall · July 28, 2026

  Ventec Life Systems, Inc.

  HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve

  Labeling; Oxygen Cylinders do not contain required medical gas labeling

  Class II

• Food Recall · July 28, 2026

  FlavorsandColor.Com

  Honeyville YELLOW COLOR 1 GALLON NFI: WATER, FD&C YELLOW #5, FD&C YELLOW #6, CITRIC ACID, AND SODIUM BENZOATE. MANUFACTURED FOR: HONEYVILLE, INC. RANCHO CUCAMONGA, CA 91730

  Undeclared Red #40.

  Class III

• Food Recall · July 28, 2026

  Wonton Specialists

  Wonton Specialist Inc. Lo Mein Noodle, 16 oz, packaged in clear plastic bags

  Undeclared FD&C Red No. 40

  Class III

• Food Recall · July 28, 2026

  Wonton Specialists

  Wonton Specialist Inc. Pan Fried Noodle, 16 oz and 5lb packaged in clear plastic bags

  Undeclared FD&C Red No. 40

  Class III

• Food Recall · July 28, 2026

  Wonton Specialists

  Wonton Specialist Inc. Cooked Noodle, 16 oz and 5 lb - packaged in clear plastic bags

  Undeclared FD&C Red No. 40

  Class III

• Food Recall · July 28, 2026

  529 COMMERCE, LLC

  Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with zipper. UPC 99284 53095 and UPC 99284 30622

  Undeclared Egg

  Class I

• Food Recall · July 27, 2026

  Elegant Foods, LLC

  Pecorino Toscano D.O.P. STAGIONATO cheese wheels. Product of Italy. Each cheese wheel is approximately 3-4 lbs. Wheels contain a wax rind. Keep Refrigerated. Produced by Soc. Cooperativa Val D'

  Potential Listeria contamination from dripping condensation in cooler.

  Class II

• Vehicle Recall · July 27, 2026

  PACCAR Incorporated

  2027 KENWORTH T680

  A loss of lighting, windshield wipers, ABS function, or a loss of drive power can increase the risk of a crash.

  Unclassified

• Medical Device Recall · July 27, 2026

  restor3d Inc.

  Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide), REF: 5831-9006

  Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation, reduced fixation or poor alignment of implants, implant loosening/migration, or need for revision surgery.

  Class II

• Medical Device Recall · July 27, 2026

  HeartSine Technologies Ltd

  HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2 Min CPR UDI-DI code: 0506016712207 350P US Device, U

  Due to a damaged (over stretched) membrane tail that causes an intermittent fault.

  Class II

• Drug Recall · July 24, 2026

  American Regent, Inc.

  AMINAOCAPROIC ACID INJECTION, USP, 250 mg/mL (5 g/20 mL), packaged in a) 20 mL MULTIPLE DOSE VIAL FOR IV INFUSION (NDC 0517-9120-01), and b) 25x20 mL MULTIPLE DOSE VIALS (NDC 0517-9120-25), Rx Only,

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II

• Drug Recall · July 24, 2026

  American Regent, Inc.

  ACETYLCYSTEINE SOLUTION, USP, 10% (100 mg/mL), packaged in a) 4 mL Vial NOT FOR INJECTION (NDC 0517-7504-01), and b) 25x4 mL Vials NOT FOR INJECTION (NDC 0517-7504-25), Rx Only, AMERICAN REGENT, INC.,

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II

• Vehicle Recall · July 24, 2026

  Mercedes-Benz USA, LLC

  2023 MERCEDES-BENZ GLB 250 4MATIC, 2024 MERCEDES-BENZ GLB 250 4MATIC, 2025 MERCEDES-BENZ AMG GLA 35, 2025 MERCEDES-BENZ GLA 250, 2025 MERCEDES-BENZ GLB 250, 2026 MERCEDES-BENZ GLB 250

  A vehicle rollaway increases the risk of a crash or injury.

  Unclassified

• Drug Recall · July 24, 2026

  American Regent, Inc.

  Atropine Sulfate injection, USP, 1 mg/mL, For intravenous Use, Sterile, packaged in a) 1 mL Single-Dose Vial (NDC 0517-1001-01), and b) 25x1 mL Single-Dose Vial (NDC 0517-1001-25), Rx only, AMERICAN R

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II

• Food Recall · July 24, 2026

  Elegant Foods, LLC

  Elegant Foods Coconut Flakes, 5 Pounds. 537 Atlas Ave, Madison, WI 53714.

  Undeclared sulfites

  Class II

• Drug Recall · July 24, 2026

  American Regent, Inc.

  Cyanocobalamin injection USP, 10,000 mcg/10 mL (1,000 mcg/mL), For IM or SC Use Only, packaged in a) 10 mL Multi-Dose Vial (NDC 0517-0032-01) and b) 25x10 mL Multi-Dose Vials (NDC 0517-0032-25), Rx On

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II

• Drug Recall · July 24, 2026

  American Regent, Inc.

  Multrys (Trace Elements Injection 4, USP), For intravenous infusion, packaged in a) 1 mL Single-Dose Vial (NDC 0517-9302-01), and b) 25x1 mL Single-Dose Vials (NDC 0517-9302-25) Rx Only, AMERICAN REGE

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II

• Drug Recall · July 24, 2026

  Mylan Pharmaceuticals Inc

  Acamprosate Calcium, Delayed-Release Tablets, 333 mg, 180 tablets bottles, Rx only, Mylan Pharmaceuticals Inc., Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 266505, NDC 0378-6333-80.

  Failed Dissolution Specifications

  Class II

• Food Recall · July 24, 2026

  Buckhead Meat Company D.B.A. Trinity Seafood

  Buckhead, Tuna, 10lb cs, 12lb cs, 15lb cs, 3-5lb cs , Styrofoam container, Keep Refrigerated

  The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.

  Class II

• Drug Recall · July 24, 2026

  American Regent, Inc.

  Selenious Acid Injection, USP 12 mcg/2 mL (6 mcg/2mL), For intravenous use, packaged in a) 2mL Single-Dose Vial (NDC 0517-6502-01), and b)10x2mL Single-Dose Vial (NDC 0517-6502-10), Rx Only, AMERICAN

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II

• Food Recall · July 24, 2026

  Elegant Foods, LLC

  Elegant Foods Carrot Cake, 9". 14 Servings. Keep Refrigerated/Frozen. 537 Atlas Ave., Madison, WI 53714.

  Carrot decoration contains Yellow #5 and Yellow #6 which is not listed on finished product label.

  Class II

• Food Recall · July 24, 2026

  Elegant Foods, LLC

  Elegant Foods Golden Raisins, 5 pound. 537 Atlas Ave, Madison, WI 53714.

  Undeclared sulfites

  Class II

• Drug Recall · July 24, 2026

  American Regent, Inc.

  Nitroglycerin injection, USP, 50 mg/10 mL (5 mg/mL), packaged in a) 10 mL vials (NDC 0517-4810-01), b) 25x10mL vials (NDC 0517-4810-25) RX only, AMERICAN REGENT, INC., Shirley, NY 11967.

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II

• Drug Recall · July 24, 2026

  American Regent, Inc.

  Cyanocobalamin injection USP, 1,000 mcg/mL, For IM or SC Use Only, packaged in a) 1 mL Multi-Dose Vial (NDC 0517-0031-01), and b) 25x1 mL Multi-Dose Vials (NDC 0517-0031-25) Rx only, AMERICAN REGENT,

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II