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. 2,369 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,369 in last 12 months

Showing 1768117700 of 47,027 recalls

DrugMay 27, 2020· Apotex Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Apotex Inc. Due...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Olanzapine Tablets Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/ Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Olanzapine Tablets Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/ Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2020· UNICHEM PHARMACEUTICALS USA INC

Recalled Item: Clonidine Hydrochloride Tablets Recalled by UNICHEM PHARMACEUTICALS USA INC...

The Issue: Failed Impurities/Degradation Specifications: potential migration of...

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

Class III — Low RiskOngoing
Refund
DrugMay 22, 2020· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Some bottles may contain mixed strengths of the product.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 30 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· The Harvard Drug Group

Recalled Item: Doxycycline Hyclate Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Dissolution Specification: The dissolution test at the 24 month time...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 90 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Some bottles may contain mixed strengths of the product.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 60 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Some bottles may contain mixed strengths of the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 22, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as Recalled...

The Issue: Lateromedial (LM) and Lateromedial Oblique (LMO) Orientation Markers may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2020· Tosoh Bioscience Inc

Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to The Substrate...

The Issue: The Substrate Monitoring System in the AIA-900 Analyzer did not detect an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2020· Vitalconnect Inc.

Recalled Item: VistaSolution Recalled by Vitalconnect Inc. Due to A healthcare provider...

The Issue: A healthcare provider (HCP) noticed a patient had a lowered historic SpO2...

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

Class II — Potential Health HazardOngoing