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. 2,348 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,348 in last 12 months

Showing 2182121840 of 47,027 recalls

Medical DeviceMarch 28, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...

The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...

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

Class I — Serious Health HazardOngoing
FoodMarch 27, 2019· Theo Chocolate Inc

Recalled Item: Sea Salt 70% Dark Chocolate 3 oz. bars Recalled by Theo Chocolate Inc Due to...

The Issue: Theo Chocolate Sea Salt 70% Dark Chocolate Bar is recalled due to undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 26, 2019· Medi-Physics Inc. dba GE Healthcare

Recalled Item: Thallous Chloride TI 201 Injection Recalled by Medi-Physics Inc. dba GE...

The Issue: Chemical Contamination: Trace amounts of an impurity was detected in the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 26, 2019· Molnlycke Health Care, Inc

Recalled Item: EZ Derm Porcine Xenograft Recalled by Molnlycke Health Care, Inc Due to...

The Issue: Intermittent heat seal failures on the outer pouch of some EZ Derm products.

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Pravastatin Sodium Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: Presence Of Foreign Tablet: in a bottle of Pravastatin Sodium Tablets 20 mg.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime SP Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Lightning Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Precision Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Vision Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Premium Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Hamilton Medical AG

Recalled Item: HAMILTON-G5 Recalled by Hamilton Medical AG Due to New software version for...

The Issue: New software version for affected ventilators reduces the probability of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: McKesson Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: Horizon Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

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

Class II — Potential Health HazardOngoing
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· Auro Pharmacies Inc. DBA Central Drugs

Recalled Item: Biotin 10 mg/mL Injection Recalled by Auro Pharmacies Inc. DBA Central Drugs...

The Issue: Failed pH Specification: product does not meet pH label claim.

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

Class III — Low RiskOngoing
Refund