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. 1,717 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
1,717 in last 12 months

Showing 3642136440 of 47,027 recalls

Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Custom Pack - with Introducer Kit Recalled by Windstone Medical Packaging,...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Cath Pack Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Percutaneous Entry Kit Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Major Lithotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Liposuction Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: GYN Lap Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: D&C/GYN/Hysteroscopy Pack Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: C-Tray Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Minor Lithotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Basic Setup Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Roche Diabetes Care, Inc.

Recalled Item: AccuChek Spirit insulin infusion pump. Recalled by Roche Diabetes Care, Inc....

The Issue: Roche has become aware of an increase of mechanical errors experienced by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Roche Diabetes Care, Inc.

Recalled Item: AccuChek Spirit Combo insulin infusion pump sold as part of Recalled by...

The Issue: Roche has become aware of an increase of mechanical errors experienced by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Alere Scarborough, Inc. dba Binax, Inc.

Recalled Item: Alere i Influenza A & B Product Usage: The Alere i Influenza A and B assay...

The Issue: High invalid rate and an increased risk of false negative results with...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Lifeline Systems, Incorporated

Recalled Item: Philips GoSafe Communicator 7000L Personal emergency response system....

The Issue: Home communicator Model 7000L may not sense the phone line under certain...

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

Class II — Potential Health HazardOngoing
DrugApril 22, 2015· Wockhardt Usa Inc.

Recalled Item: Azithromycin Tablets Recalled by Wockhardt Usa Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2015· Wockhardt Usa Inc.

Recalled Item: Lisinopril Tablets USP Recalled by Wockhardt Usa Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2015· Wockhardt Usa Inc.

Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Wockhardt Usa Inc. Due to...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2015· Wockhardt Usa Inc.

Recalled Item: Amlodipine Besylate Tablets Recalled by Wockhardt Usa Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2015· Wockhardt Usa Inc.

Recalled Item: Zonisamide Capsules Recalled by Wockhardt Usa Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2015· Wockhardt Usa Inc.

Recalled Item: Famotodine Tablets Recalled by Wockhardt Usa Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund