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. 2,313 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,313 in last 12 months

Showing 3312133140 of 47,027 recalls

Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Hill-Rom, Inc.

Recalled Item: Hill-Rom Bariatric Power Recliner Recalled by Hill-Rom, Inc. Due to The...

The Issue: The recliners were shipped without the foot rest ottoman linkage side...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2016· Sorin Group USA, Inc.

Recalled Item: CDI H/S Cuvette Recalled by Sorin Group USA, Inc. Due to The CDI System 500...

The Issue: The CDI System 500 monitor displays the "H/S DISCONNECT AT CUVETTE" error...

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

Class III — Low RiskOngoing
DrugJanuary 18, 2016· Perrigo Company PLC

Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...

The Issue: Labeling: label error on declared strength.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Perrigo Company PLC

Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...

The Issue: Labeling: label error on declared strength.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Cyclopentolate Hydrochloride Ophthalmic Solution USP Recalled by Bausch &...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Amerisource Health Services

Recalled Item: Levofloxacin Tablets USP Recalled by Amerisource Health Services Due to...

The Issue: Failed Dissolution Specifications: Unexplained low out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: A Picture Archiving and Communication System (PACS) intended to display...

The Issue: To inform users about the possible incorrect values for Distance...

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

Class II — Potential Health HazardOngoing