Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,521 recalls have been distributed to Vermont in the last 12 months.
Showing 4981–5000 of 47,027 recalls
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cepheid Recalled by Cepheid Due to Specimen collection device may leak after...
The Issue: Specimen collection device may leak after the patient sample swabs have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test Recalled by...
The Issue: Potential for defective test cartridges which may result in false positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...
The Issue: If blood culture identification panel is used in conjunction with specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELFLEX PERITONEAL DIALYSIS SOLUTION With LOW MAGNESIUM / LOW CALCIUM...
The Issue: This product is being recalled due to the tube weld failure presents itself...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dodex Injectable (Cyanocobalamin Injection) USP Recalled by Accord...
The Issue: Subpotent drug: out of specification results
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Recalled by The Harvard Drug Group LLC dba Major...
The Issue: Failed dissolution specifications: out of specification result obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...
The Issue: Two (2) reports were sent to customers with an incorrect negative claim on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOFT-VU KUMPE 5F X 40CM -Used for patients in need Recalled by...
The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOFT-VU KUMPE 5F X 65CM -Used for patients in need Recalled by...
The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count Recalled by Embecta Corp. Due...
The Issue: BD Nano 2nd Gen Pen Needle was shipped close to or after the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.