Latest recalls — page 28
Older notices, newest first.
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Class II · last month
Windstone Medical Packaging, Inc. AMS Convenience Kit: DSAEK Pack - RX recall: The convenience kits contain .0.9% Sodium Chloride Injection
The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts…
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Class II · last month
Nipro Renal Soultions USA, Corporation MedicaLyte Bicarbonate Powder REF: DB+201-2.1 recall: Hemodialysis concentrates contain high endotoxin levels
Hemodialysis concentrates contain high endotoxin levels
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Class II · last month
C.R. Bard Inc Products that contain the Pericare Wipes: SureStep" Foley Tray System recall: Due to complaints received indicating presence of contamination
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent…
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Class II · last month
Nipro Renal Soultions USA, Corporation Citric Complete Liquid Citric Acid Concentrate recall: Hemodialysis concentrates contain high endotoxin levels
Hemodialysis concentrates contain high endotoxin levels
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Class II · last month
Atrium Medical Corporation Getinge PVC Thoracic Catheter, Firm PVC Straight recall: An Out of Specification result (OOS) related to bacterial endotoxin testing
An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.
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Class II · last month
C.R. Bard Inc Products that contain the Pericare Wipes: Bardex Lubricath Foley recall: Due to complaints received indicating presence of contamination
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent…
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Class II · last month
HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes recall: Due to a damaged (over stretched) membrane tail that causes an intermittent
Due to a damaged (over stretched) membrane tail that causes an intermittent fault.
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Class II · last month
C.R. Bard Inc Products that contain the Pericare Wipes: Bard¿ Foley Tray recall: Due to complaints received indicating presence of contamination
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent…
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Class II · last month
Atrium Medical Corporation Getinge PVC Thoracic Catheter, Soft PVC Straight recall: An Out of Specification result (OOS) related to bacterial endotoxin testing
An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.
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Class II · last month
C.R. Bard Inc Products that contain the Pericare Wipes: SureStep" Foley Tray System recall: Due to complaints received indicating presence of contamination
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent…
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Class II · last month
Lutronic Corporation Product Name: DermaV Laser System Model/ recall: Utilizing higher fluences at 1064nm wavelength with current cryogen
Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially…
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Class II · last month
Nipro Renal Soultions USA, Corporation MedicaLyte Liquid Bicarbonate Concentrate REF recall: Hemodialysis concentrates contain high endotoxin levels
Hemodialysis concentrates contain high endotoxin levels
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Class I · last month
B Braun Medical Inc 0.9% Sodium Chloride Injection, USP recall: Presence of Particulate Matter: particulate matter identified as iron oxide
Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene
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Class I · last month
Baxter Healthcare Corporation Dextrose Injection, USP, 70 %, 2000 mL bags recall: Presence of Particulate Matter: particulate matter identified as stainless
Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.
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Class III · last month
Ajanta Pharma USA Inc Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles recall: Failed impurities/degradation specifications: (OOS) for Organic Impurities
Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability…
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Class I · last month
American Regent, Inc. Epinephrine Injection, USP, 30 mg/30 mL recall: Presence of Particulate Matter and Lack of Assurance of Sterility
Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and…
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Class III · last month
ImprimisRx NJ LLC Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution recall: Subpotent Drug
Subpotent Drug
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Class II · last month
OurPharma LLC fentaNYL Citrate, 1,000 mcg/100 mL Injection solution in 100 mL recall: Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026
Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and…
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Class II · last month
Ferrero USA Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz recall: Undeclared milk and pecans
Undeclared milk and pecans
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Class I · last month
International Sprout Holdings, Inc Alfalfa, Net Weight 50 lbs. bag, Product of USA recall: Potential E. coli and Salmonella contamination
Potential E. coli and Salmonella contamination
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Class I · last month
Exotique Foods Canada Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower recall: Undeclared Wheat
Undeclared Wheat.
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Class II · last month
L-Nutra Inc Prolon Everyday Apulian Almond & Cocoa Spread recall: Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio
Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.
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Class I · last month
Euro Foods Group USA Nj Inc Crown Farms Dried Suri Cut, 200 gm, in plastic pack recall: The firm imported and distributed dried ribbon fish that was not properly
The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.
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NHTSA safety recall · last month
Volkswagen Tiguan recall: A software error may cause the body control module (BCM) system to reset
A software error may cause the body control module (BCM) system to reset. This may result in the ignition switching off, resulting in an engine…