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. 2,541 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,541 in last 12 months

Showing 28012820 of 47,027 recalls

DrugFebruary 28, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Sigan Industries Group Inc.

Recalled Item: Walgreens Recalled by Sigan Industries Group Inc. Due to Chemical...

The Issue: Chemical Contamination: Presence of benzene

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 28, 2025· Reichert, Inc.

Recalled Item: Phoroptor VRx Digital System Model Numbers: 16241 Recalled by Reichert, Inc....

The Issue: The head of the phoropter head could come loose and potentially detach due...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Reichert, Inc.

Recalled Item: Phoroptor VRx Digital System Model Numbers: 16242 Recalled by Reichert, Inc....

The Issue: The head of the phoropter head could come loose and potentially detach due...

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

Class II — Potential Health HazardOngoing
DrugFebruary 27, 2025· Amgen, Inc.

Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...

The Issue: Stability data does not support expiry: the products have the potential to...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 27, 2025· Amgen, Inc.

Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...

The Issue: Stability data does not support expiry: the products have the potential to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2025· Premier Dental Products Co

Recalled Item: Premier Solo Diamond - Large Invented Cone Recalled by Premier Dental...

The Issue: The hardness not meeting the material specification and may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2025· Zimmer, Inc.

Recalled Item: NexGen LPS Flex Recalled by Zimmer, Inc. Due to The "Use with plate 7, 8, 9,...

The Issue: The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2025· Beckman Coulter Inc.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...

The Issue: Beckman Coulter has determined that device software versions V1.3, V1.4,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2025· Intuitive Surgical, Inc.

Recalled Item: Brand Name: Da Vinci 5 Product Name: ASSY Recalled by Intuitive Surgical,...

The Issue: Due to an increase in complaints concerning foot tray pedal spring failing...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2025· A-S Medication Solutions LLC

Recalled Item: METFORMIN HYDROCHLORIDE EXTENDED- RELEASE 500MG Recalled by A-S Medication...

The Issue: Presence of Foreign Tablets/Capsules.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2025· MYLAN PHARMACEUTICALS INC

Recalled Item: Prasugrel Tablets Recalled by MYLAN PHARMACEUTICALS INC Due to Failed...

The Issue: Failed Dissolution Specifications - low dissolution results

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Otopore Cylinder outer ear wound dressing Recalled by Stryker Corporation...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore FD fragmentable nasal dressing Recalled by Stryker Corporation Due...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Otopore Square outer ear wound dressing Recalled by Stryker Corporation Due...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Hemopore 8cm nasal/sinus temporary wound dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Hemopore 2PK nasal/sinus temporary wound dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Standard 8cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 8cm fragmentable nasal dressing Recalled by Stryker Corporation Due...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing