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. 1,641 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
1,641 in last 12 months

Showing 4338143400 of 47,027 recalls

DrugMay 20, 2013· Hospira, Inc.

Recalled Item: Ondansetron Injection Recalled by Hospira, Inc. Due to Presence of...

The Issue: Presence of Particulate; lot being recalled as a precaution due to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 20, 2013· Dolphin Intertrade Corporation

Recalled Item: XIYOUJI QINGZHI CAPSULE Recalled by Dolphin Intertrade Corporation Due to...

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
DrugMay 17, 2013· Warner Chilcott US LLC

Recalled Item: Enablex (darifenacin) Extended Release Tablet Recalled by Warner Chilcott US...

The Issue: Failed Impurities/Degradation Specifications: unspecified degradation product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 17, 2013· SpineFrontier, Inc.

Recalled Item: BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case...

The Issue: The S-LIFT Instrument Case contained a bracket with peeling nylon coating.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2013· RF Technologies, Inc.

Recalled Item: Code Alert Advanced 4-Way Care Solution Recalled by RF Technologies, Inc....

The Issue: RF Technologies, Inc. has initiated a recall involving CA520 Code Alert...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Pro System The CoaguChek XS Pro System (CoaguChek Recalled by...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS System (PST) The CoaguChek XS PT test strips Recalled by Roche...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS System (HCP) The CoaguChek XS System is intended Recalled by...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· The Standing Company

Recalled Item: Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device...

The Issue: Power Superstand Standing Wheel chair, flex shaft (the flexible wand which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Plus System The CoaguChek XS Plus system for Recalled by Roche...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
FoodMay 16, 2013· Chs Inc

Recalled Item: Solcon Soy Protein Concentrates. Item No. / Item Description: 12110 Recalled...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2013· Chs Inc

Recalled Item: Solbar Q Soy Protein Isolates. Item No. / Item Description: Recalled by Chs...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 16, 2013· Chs Inc

Recalled Item: Contex - Textured Soy Protein Concentrates Item No. / Item Recalled by Chs...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class II — Potential Health HazardOngoing
Refund