Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,853 recalls, newest first · Checked 0 minutes ago
United StatesGreiner Bio-One North America, Inc. recalls Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Clot Activator Model/Catalog…
Some of the Vacuette¿ CAT Serum Separator Clot Activator tubes were manufactured without gel separator, which could yield erroneous assay results and require the…Medtronic Perfusion Systems recalls MC3 VitalFlow Console
As of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consoles displaying an E70 error code during normal operation.Olympus Corporation of the Americas recalls Brand Name: EZDilate Nephrostomy Balloon Catheter and Inflation Device Kit Product Name…
Device kits contained an incorrectly sized 4mm x 4cm urinary tract balloon catheter (BURS0404) instead of the correct 8mm x 15cm nephrostomy tract balloon catheter…Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC recalls OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials…
A labeling error was identified on the affected product.Medtronic Perfusion Systems recalls Medtronic HR-ACT
Medtronic personnel observed trace amounts of dry blood on the external carton label and Instructions for Use (IFU) in five boxes of one lot of ACT Cartridges.Meridian Bioscience Inc recalls Meridian Bioscience and 1 more products
The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume.Exactech, Inc. recalls Brand Name: Equinoxe Ergo Product Name: Adjustable Angle rTSA Reamer and 2 more products
Due to products that have not completed design updates and performance testing being released/distributed.Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System and 3 more products
Due to potential corrosion issues associated with the Backup Battery cable connector that may cause a Backup Battery Fault Alarm.CareFusion 303, Inc. recalls BD Alaris infusion Pump Module 8100
If infusion pump is dropped or severely jarred this may damage the pump module bezel assembly, which can cause under-infusion, over-infusion, unregulated flow, or pump…Cellavision AB recalls REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60
Automated cell-locating device barcode reader may read the barcode of the previously processed slide resulting in a misattribution of diagnostic results.ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection and 23 more products
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.Medline Industries, LP recalls MEDLINE convenience kits labeled as LOCAL BASIC and 19 more products
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils.Alembic Pharmaceuticals Limited recalls Fesoterodine Fumarate
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.Imprimis NJOF, LLC recalls Klarity-C Drops
Subpotent DrugZydus Pharmaceuticals (USA) Inc recalls Bromocriptine Mesylate Capsules
Failed Impurities/Degradation Specifications: Out of Specification (OOS) result reported for 2- Bromoergine impurity of Bromocriptine Mesylate Capsules.Park Avenue Compounding recalls Fentanyl citrate
CGMP Deviations: Revised interpretation of Acceptable Quality Level (AQL) results.Otsuka ICU Medical LLC recalls POTASSIUM CHLORIDE Inj. and 1 more products
Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj.Golden State Medical Supply Inc. recalls NIACIN Extended-Release Tablets
Failed Dissolution SpecificationsDermaRite Industries, LLC recalls 4-N-1 Skin Protectant and 17 more products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.Plenus Group Inc. recalls Rockport Lobser Bisque
Products contain undeclared shrimp (crustacean shellfish)Haitai, Inc. recalls Cinnamon Powder
Elevated levels of lead in Cinnamon powder.Publix Super Markets, Inc. recalls Publix Rich & Creamy Vanilla Ice Cream
Undeclared EggsBulk & Organic LLC recalls Bulk and Organic Organic Moringa Powder
Possible Salmonella RichmondA little guidance
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