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. 2,369 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,369 in last 12 months

Showing 1762117640 of 47,027 recalls

DrugJune 4, 2020· SOMERSET THERAPEUTICS LLC

Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...

The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 4, 2020· SOMERSET THERAPEUTICS LLC

Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...

The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 4, 2020· SOMERSET THERAPEUTICS LLC

Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...

The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 4, 2020· AVKARE Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 4, 2020· AVKARE Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Cardinal Health 200, LLC

Recalled Item: Cardinal Health NPWT Canister with Gel 300cc Recalled by Cardinal Health...

The Issue: Canisters potentially contain an oversized O-ring that cannot be installed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Cardinal Health 200, LLC

Recalled Item: Cardinal Health NPWT Occlusion Detection Canister 300cc Recalled by Cardinal...

The Issue: Canisters potentially contain an oversized O-ring that cannot be installed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 3, 2020· A.P. Deauville, LLC

Recalled Item: Soft Whisper by Powerstick Dandruff Shampoo (Pyrithione Zinc) Recalled by...

The Issue: cGMP Deviations: Soft Whisper Dandruff Shampoo was produced with water that...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJune 3, 2020· Toufayan Bakery, Inc.

Recalled Item: TOUFAYAN BAKERIES SMART POCKETS EVERYTHING 6 COUNT NET WT 7.4 OZ. (210 g)...

The Issue: Undeclared sesame seeds, poppy seeds, and dehydrated garlic.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 3, 2020· LONGHORN VACCINES AND DIAGNOSTIC

Recalled Item: PrimeStore Molecular Transport Medium (PS-MTM) Recalled by LONGHORN VACCINES...

The Issue: The tubes may have been delivered to some users without labels. Users may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing