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. 2,503 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,503 in last 12 months

Showing 72417260 of 47,027 recalls

Medical DeviceOctober 25, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use only....

The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2023· GRAPHENANO DENTAL SL

Recalled Item: GRAPHENANO DENTAL G-CAM Recalled by GRAPHENANO DENTAL SL Due to Machining...

The Issue: Machining error on cams renders the device unusable.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: Liberty Select Cycler Recalled by Fresenius Medical Care Holdings, Inc. Due...

The Issue: Affected Liberty Select cyclers may display an incorrect time stamp on the...

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

Class III — Low RiskOngoing
Medical DeviceOctober 24, 2023· Karl Storz Endoscopy

Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...

The Issue: The efficacy of the manual cleaning process cannot be assured for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2023· Karl Storz Endoscopy

Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...

The Issue: The efficacy of the manual cleaning process cannot be assured for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2023· Karl Storz Endoscopy

Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...

The Issue: The efficacy of the manual cleaning process cannot be assured for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2023· Karl Storz Endoscopy

Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...

The Issue: The efficacy of the manual cleaning process cannot be assured for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2023· Karl Storz Endoscopy

Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...

The Issue: The efficacy of the manual cleaning process cannot be assured for the...

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

Class II — Potential Health HazardOngoing
DrugOctober 23, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Phenytoin Oral Suspension Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed Content Uniformity Specifications

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 23, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by Glenmark...

The Issue: Failed Impurities/Degradation Specifications:Out of Specification result...

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

Class III — Low RiskOngoing
Refund
DrugOctober 23, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Ranolazine Extended-Release Tablets 500mg Recalled by Glenmark...

The Issue: Failed Dissolution Specifications: Out of specification for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Ingenia 1.5T CX Recalled by Philips North America Llc Due to Potential...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Initial System Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Intera 1.5T Power/Pulsar Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Intera 1.5T Recalled by Philips North America Llc Due to Potential component...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
DrugOctober 20, 2023· Botanical Be

Recalled Item: Artri King con Origa y Omega 3 tablets Recalled by Botanical Be 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
DrugOctober 20, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled by Glenmark...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund