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. 2,332 recalls have been distributed to Vermont in the last 12 months.
Showing 25681–25700 of 47,027 recalls
Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G....
The Issue: Package integrity failure observed during routine shift package integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmunoCAP Allergen c5 Recalled by Phadia US Inc Due to The stability...
The Issue: The stability specifications of ImmunoCAP Allergen c5, Ampicilloyl were not met.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmunoCAP Allergen c6 Recalled by Phadia US Inc Due to The stability...
The Issue: The stability specifications of ImmunoCAP Allergen c6, Amoxicilloyl were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: c6000 Recalled by Roche Diagnostics Corporation Due to Complaints have been...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 411 Immunoassay Analyzer (Discrete Photometric Analyzer for Clinical...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular E 170 Analyzer: Immunoassay Chemistry Analyzer Recalled by Roche...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fosphenytoin Sodium Injection Recalled by Amneal Pharmaceuticals Due to...
The Issue: Presence of particulate matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Oral Solution Recalled by Akorn Inc Due to CGMP Deviations:...
The Issue: CGMP Deviations: Inadvertent release of a drug product with unapproved...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.25% Acetic Acid Irrigation USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: identified as polyethylene, which is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Uterine Electromyographic Monitor -Monica IF24 Interface System Product...
The Issue: if the cables of the Monica IF24 System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uterine Electromyographic Monitor - Monica Novii Wireless Patch System...
The Issue: if the cables of the Monica Novii System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Model 882480 Product Usage: BrightView and BrightView X are...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.