Product Recalls in Connecticut

Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,461 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,461 in last 12 months

Showing 2064120660 of 28,245 recalls

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 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· 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· Zimmer Biomet, Inc.

Recalled Item: Herga foot switch Recalled by Zimmer Biomet, Inc. Due to Complaints were...

The Issue: Complaints were received reporting the system would freeze/shut down while...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Magellan Diagnostics, Inc.

Recalled Item: LeadCare II Blood Lead Test Kit Recalled by Magellan Diagnostics, Inc. Due...

The Issue: LeadCare II Test Kits controls out of range

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

Class II — Potential Health HazardOngoing