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 2112121140 of 28,245 recalls

Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Hex Try-in Screw (5 pk) Dental implants Recalled by Biomet 3i, LLC...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: DAL-RO Threaded Female Dental implants Recalled by Biomet 3i, LLC Due to...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: O-Ring Abutment 4.1mm(D) x 2mm(H) Item: OSO20 Dental implants Recalled by...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Locator Extra Light Retention Males 4pk Dental implants Recalled by Biomet...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Implant EP Twist Lock TM Coping Dental implants Recalled by Biomet...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare PIIC Classic Upgrade Recalled by Philips Electronics...

The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Conical Abutment Pick-up Coping Dental implants Recalled by Biomet 3i, LLC...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare IntelliVue Info Center iX Recalled by Philips Electronics...

The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Locator Abutment Impression Coping Dental implants Recalled by Biomet 3i,...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Standard Abutment Dental implants Recalled by Biomet 3i, LLC Due to Pouches...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Gingihue 15 degree Angled Post 4.1mm(D) x 5mm(P) x Recalled by...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: LDA Screw SBL 4mm(D) Item: SCRSBL2 Dental implants Recalled by Biomet 3i,...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Temporary Non-Hexed Cylinder Dental implants Recalled by Biomet 3i,...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Preformance 15 degrees pre-angled post Dental implants Recalled by Biomet...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain EP Twist Lock TM Coping Dental implants Recalled by Biomet 3i, LLC...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare IntelliVue Info Center iX Recalled by Philips Electronics...

The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: IOL Pick-Up Impression Coping Dental implants Recalled by Biomet 3i, LLC Due...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Standard Abutment Transfer Coping Dental implants Recalled by Biomet 3i, LLC...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Standard Abutment Temporary Screw Dental implants Recalled by Biomet 3i, LLC...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Locator Replacement Housing Dental implants Recalled by Biomet 3i, LLC Due...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing