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. 2,503 recalls have been distributed to Vermont in the last 12 months.
Showing 7261–7280 of 47,027 recalls
Recalled Item: Reumo Flex caplets Recalled by Botanical Be Due to Undeclared Diclofenac
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kuka Flex Forte caplets Recalled by Botanical Be Due to Undeclared Diclofenac
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Deferasirox Tablets for Oral Suspension Recalled by Glenmark Pharmaceuticals...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxaydo (oxycodone HCl Recalled by Zyla Life Sciences US Inc. Due to...
The Issue: Sub-potent Drug: Lower potency than labeled.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Opium Tincture Recalled by Edenbridge Pharmaceuticals, LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Item 19858 Recalled by GIVE AND GO PREPARED FOODS CORP Due to Potential...
The Issue: Potential plastic pieces in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Strong Iodine Solution U.S.P. (Lugol's Solution) (Iodine 5%) Recalled by...
The Issue: CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Processing Module The Alinity c Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 Processing Module 02P24-02 02P24-40 01R24-56 01R25-56...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Blood Analysis System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed a potential issue that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Clean Stool Transportation System-For the collection...
The Issue: Due to a manufacturing defect, certain Para-Pak vials may be at risk for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Para-Pak Zn-PVA/10% Formalin-for the routine collection Recalled by Meridian...
The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Para-Pak Clean Vial-For the collection Recalled by Meridian Bioscience Inc...
The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit - For access to the subarachnoid Recalled by...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.