Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,348 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,348 in last 12 months

Showing 3418134200 of 48,219 recalls

Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Twist Lock TM 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: Certain IOL Abutment 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: Certain Conical Abutment 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: 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: 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· 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: Pick-Up Impression Coping 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: Temporary Non-Hexed Cylinder 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: Locator Extra Light Angled Replacement Males 4pk 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: Certain Provide Abutment 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: Cover Screw Recalled by Biomet 3i, LLC Due to Pouches may not have been...

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 Preformance Post 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: 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: 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· 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· 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: Gold -Tite Hexed Retaining 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· 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· Abeon Medical Corporation

Recalled Item: TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) Recalled...

The Issue: The firm was notified by some of their customers that some of the sealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter Recalled by...

The Issue: Potential for separation of the proximal handle from the shaft.

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

Class II — Potential Health HazardOngoing