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. 2,356 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,356 in last 12 months

Showing 4910149120 of 51,038 recalls

FoodSeptember 25, 2012· Chattanooga Bakery Inc

Recalled Item: Moon Pie(R) Crunch Peanut Butter Recalled by Chattanooga Bakery Inc Due to...

The Issue: Peanut Butter Crunch Moon Pies were manufactured with peanut butter supplied...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 25, 2012· Stryker Communications, Inc.

Recalled Item: (l) Visum Halogen Surgical Light Recalled by Stryker Communications, Inc....

The Issue: Stryker has become aware that there is a low likelihood of incomplete...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Alphatec Spine, Inc.

Recalled Item: ILLlCO¿ MIS Posterior Fixation System Recalled by Alphatec Spine, Inc. Due...

The Issue: The firm initiated the recall because the stainless steel guide-wire of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Belmont Instrument Corporation

Recalled Item: Belmont Rapid Infuser Recalled by Belmont Instrument Corporation Due to Leak...

The Issue: Leak from a saline bag caused saline to drip along the back of the Rapid...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Teleflex Medical

Recalled Item: Hem-o-lok Large Polymer Ligating Clips Recalled by Teleflex Medical Due to...

The Issue: Product is being recalled due to the possibility that the tray may contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Battery Recalled by Terumo Cardiovascular Systems Corporation Due to Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Battery Recalled by Terumo Cardiovascular Systems Corporation Due to Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Winco Mfg., LLC

Recalled Item: PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...

The Issue: The performance of the chemicals in the foam and vinyl are not consistent...

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

Class II — Potential Health HazardOngoing