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. 1,648 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
1,648 in last 12 months

Showing 4242142440 of 47,027 recalls

DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: B-50 capsules Recalled by Mira Health Products Ltd. Due to Marketed without...

The Issue: Marketed without an Approved NDA/ANDA; product found to contain methasterone...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 22, 2013· Torrent Pharma Inc

Recalled Item: Olanzapine Tablets Recalled by Torrent Pharma Inc Due to Defective...

The Issue: Defective Container; This action is being taken as a precautionary measure...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: Super-DMZ Rx 2.0 Capsules Recalled by Mira Health Products Ltd. Due to...

The Issue: Marketed without an Approved NDA/ANDA; product contains the steroid...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Watson Laboratories Inc

Recalled Item: Oxycodone and Acetaminophen Capsules Recalled by Watson Laboratories Inc Due...

The Issue: Subpotent drug: Two lots of Oxycodone and Acetaminophen Capsules, USP 5/500...

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

Class III — Low RiskOngoing
Refund
DrugJuly 19, 2013· Myson Corporation, Inc.

Recalled Item: Volcano Male Enhancement 1500mg Recalled by Myson Corporation, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Man Herbal Blend With L-Carnitine Dietary Supplement Recalled by...

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.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Fem Mezcla con L-Carnitina Suplemento Alimenticio Recalled by...

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.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelin Siloutte Te Recalled by Herbal Give Care Llc Due to Undeclared...

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.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelin Siloutte Mezcal Herbal con L-Carnitine Suplemento Alimenticio...

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.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Siloutte Suplemento Alimenticio Recalled by Herbal Give Care Llc...

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.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Bracco Diagnostics Inc

Recalled Item: Tagitol V Barium Sulfate Suspension (40% w/v Recalled by Bracco Diagnostics...

The Issue: Failed Stability Specifications: Tagitol V Barium Sulfate Lot #65846 sampled...

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

Class III — Low RiskOngoing
Refund
DrugJuly 19, 2013· Myson Corporation, Inc.

Recalled Item: Volcano Male Enhancement Liquid Recalled by Myson Corporation, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR V-Patch Mesh (All sizes and shapes). Intended for use Recalled by...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR TacShield Mesh (All sizes and shapes). Intended for use Recalled by...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 300 and ACL TOP 300 CTS (Japan) Recalled by Instrumentation...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Edge Mesh (All sizes and shapes). Intended for use Recalled by Atrium...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing