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. 2,332 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,332 in last 12 months

Showing 2690126920 of 47,027 recalls

Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: NON-STERILE SAMPLE Recalled by Sorin Group USA, Inc. Due to Medtronic...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: NON-STERILE SAMPLE Recalled by Sorin Group USA, Inc. Due to Medtronic...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: NON-STERILE SAMPLE Recalled by Sorin Group USA, Inc. Due to Medtronic...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: STERILE SAMPLE SORIN GROUP Recalled by Sorin Group USA, Inc. Due to...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: Obagi-C Rx System C-Therapy Night Cream Recalled by Valeant Pharmaceuticals...

The Issue: Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy...

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2017· GSK Consumer Healthcare

Recalled Item: parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and...

The Issue: Presence of Foreign Substance: possibility of the presence of metal in the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 27, 2017· Peanut Butter holdings, LLC

Recalled Item: PB Crave Recalled by Peanut Butter holdings, LLC Due to Mislabeling

The Issue: Product mislabeled. "'Contains " allergen statement under the ingredient...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle Recalled...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety Deluxe Bone Marrow Biopsy/Aspiration Tray Recalled by Robert Busse &...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing