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. 2,244 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,244 in last 12 months

Showing 4358143600 of 47,027 recalls

Medical DeviceApril 25, 2013· Leibel-Flarsheim Company LLC

Recalled Item: Hydra Vision DR 60/80 System Recalled by Leibel-Flarsheim Company LLC Due to...

The Issue: A complaint was received in which a hospital physicist indicated the dosage...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: B-CrossLaps/serum (B-CTx in serum) 160 100 tests Immunoassay Recalled by...

The Issue: Roche Diagnostics internal investigations in R&D have shown that the claims...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight2 Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
DrugApril 24, 2013· Insight Instruments, Inc.

Recalled Item: Cornea Coat Recalled by Insight Instruments, Inc. Due to Marketed without an...

The Issue: Marketed without an Approved NDA/ANDA.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 24, 2013· Embla System Llc

Recalled Item: embla Embletta Gold (It functions as a Polysomnography Recorder and Recalled...

The Issue: Calibration error for Embla Embletta Gold units calibrated through service...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Glutathione 200mg/ml Inj SDV: 3x50ml 14 day expiration Recalled by Nora...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Vancomycin Opth Soln14mg/ml PF Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Tobramycin Opth Soln 14mg/ml Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: PGE-1 Inj 40mcg/ml MDV Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Renacidin Irrigation: 1000 ml Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Papaverine Inj 30mg/ml Syr Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Ropinirole hydrochloride tablets Recalled by Mylan Pharmaceuticals Inc. Due...

The Issue: Labeling: Label Error on Declared Strength- Unopened bottles of Ropinirole...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Tobramycin Opth Soln 13mg/ml Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2013· Nora Apothecary and Alternative Therapies, Inc.

Recalled Item: Trimix Inj 30:1:40 MDV Recalled by Nora Apothecary and Alternative...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund