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. 2,508 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,508 in last 12 months

Showing 66216640 of 47,027 recalls

Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 1.5T. Model (REF) Numbers 781196 Recalled by Philips North America...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva XR. Model (REF) Numbers 781153 Recalled by Philips North America Due...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 1.5T Initial system. Model (REF) Numbers 781178. Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Ingenia 1.5T CX. Model (REF) Numbers 781262 Recalled by Philips North...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 3.0T. Model. (REF) Numbers 781277 Recalled by Philips North America...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Intera Achieva 1.5T Pulsar. Model (REF) Number 781171. Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 1.5T Conversion. Model (REF) Numbers 781346 Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173. Recalled by...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: SmartPath to dStream for 1.5T. Model (REF) Numbers 781260 Recalled by...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
FoodJanuary 2, 2024· Stonewall Kitchen, LLC

Recalled Item: Vermont Village Unsweetened Apple Sauce (24oz) Recalled by Stonewall...

The Issue: Product contains elevated levels of patulin.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tizanidine Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Presence of Foreign tablets/capsules - identified as tizanidine 2 mg tablets.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Framegrabber card may not perform as intended. Monitor may show no...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Framegrabber card may not perform as intended. Monitor may show no...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Disk Bay may not perform as intended. System may stop functioning and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Disk Bay may not perform as intended. System may stop functioning and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· Zimmer Surgical Inc

Recalled Item: 3:1 Dermacarrier Recalled by Zimmer Surgical Inc Due to Due to manufacturing...

The Issue: Due to manufacturing issue, the product is labeled as 3:1 ratio, but the...

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

Class II — Potential Health HazardOngoing
FoodDecember 30, 2023· Mead Johnson & Company LLC

Recalled Item: Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6...

The Issue: Product has the potential to be contaminated with Cronobacter sakazakii.

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 29, 2023· Strides Pharma Inc.

Recalled Item: Methoxsalen Capsules Recalled by Strides Pharma Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 29, 2023· Ascend Laboratories, LLC

Recalled Item: Ibuprofen and Famotidine Tablets 800mg/26.6mg Recalled by Ascend...

The Issue: Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet...

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

Class II — Potential Health HazardOngoing
Refund