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. 1,023 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
1,023 in last 12 months

Showing 16161–16180 of 47,027 recalls

Medical DeviceNovember 23, 2020· GE Healthcare, LLC

Recalled Item: Revolution CT with Apex Edition CT System - Product Usage: intended for head...

The Issue: A potential for protocol(s) with unintended patient orientation or scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Diasorin Inc.

Recalled Item: LIAISON 1-84 PTH Assay - Product Usage: is an in Recalled by Diasorin Inc....

The Issue: Potential for system to produce falsely elevated parathyroid hormone (PTH)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Citrasate Liquid Acid concentrate drums Recalled by Fresenius Medical Care...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate drums Recalled by Fresenius Medical Care...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
DrugNovember 23, 2020· Ascend Laboratories LLC

Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...

The Issue: Failed Impurity/Degradation Specifications: Unidentified impurities not...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2020· Complete Pharmacy and Medical Solutions, LLC.

Recalled Item: HUMAN CHORIONIC GONADOTROPIN 1 Recalled by Complete Pharmacy and Medical...

The Issue: CGMP deviations: Lack of potency testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2020· Complete Pharmacy and Medical Solutions, LLC.

Recalled Item: HUMAN CHORIONIC GONADOTROPIN 11 Recalled by Complete Pharmacy and Medical...

The Issue: CGMP deviations: Lack of potency testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2020· Complete Pharmacy and Medical Solutions, LLC.

Recalled Item: HUMAN CHORIONIC GONADOTROPIN 6 Recalled by Complete Pharmacy and Medical...

The Issue: CGMP deviations: Lack of potency testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2020· Complete Pharmacy and Medical Solutions, LLC.

Recalled Item: HUMAN CHORIONIC GONADOTROPIN 5 Recalled by Complete Pharmacy and Medical...

The Issue: CGMP deviations: Lack of potency testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2020· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: Scandonest 3% Plain (Mepivacaine Hydrochloride 3% without Vasoconstrictor)...

The Issue: Labeling: Label mix-up

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

Class III — Low RiskOngoing
Refund
FoodNovember 20, 2020· Riverside Natural Foods, Ltd.

Recalled Item: Good & Gather Banana Chocolate Chip Date & Nut Bars Recalled by Riverside...

The Issue: The product contains an undeclared almonds.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 20, 2020· Zimmer Biomet, Inc.

Recalled Item: Spinal Rod Cutter Recalled by Zimmer Biomet, Inc. Due to Device has the...

The Issue: Device has the potential for fracture during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Automation Solutions Recalled by Ortho-Clinical Diagnostics, Inc. Due...

The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Ortho-Clinical Diagnostics, Inc.

Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics,...

The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS Set Advanced Recalled by Maquet Cardiovascular Us Sales, Llc Due to The...

The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS Set Advanced Model Name: BEQ-HLS 5050 USA Recalled by Maquet...

The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Haag-Streit USA Inc

Recalled Item: Haag Streit Surgical Floor stands FS 2-11 (. 615H511) Recalled by...

The Issue: Software error -Software 588 versions 2.0 to 3.3, movement of the focusing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 11.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 17.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Steris Corporation

Recalled Item: Medisafe Distal Duck Kit and Duck Bag Recalled by Steris Corporation Due to...

The Issue: STERIS has identified that certain lots of diluted 4-Zyme may contain...

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

Class II — Potential Health HazardOngoing