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. 2,330 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,330 in last 12 months

Showing 3978139800 of 48,219 recalls

Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA The Personalized Knee System PS Tibial Articular Surface Provisional...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA The Personalized Knee System CR Tibial Articular Surface Provisional...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA The Personalized Knee System Constrained Tibial Articular Surface...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA The Personalized Knee System Constrained Posterior Stabilized Tibial...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA The Personalized Knee System Tibial Articular Surface Provisional...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
DrugAugust 6, 2014· Qualitest Pharmaceuticals

Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...

The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2014· Qualitest Pharmaceuticals

Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...

The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2014· Qualitest Pharmaceuticals

Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...

The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2014· Sedecal S.A.

Recalled Item: MobileDiagnost wDR motorized portable diagnostic X-ray systems. Recalled by...

The Issue: Reports of unexpected movement.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Parker Laboratories, Inc.

Recalled Item: Parker Eclipse Probe Cover Recalled by Parker Laboratories, Inc. Due to...

The Issue: Parker Laboratories, Inc. received a report of an incorrect expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Arrow International Inc

Recalled Item: Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) Recalled...

The Issue: The component supplier recalled their 0.9% Sodium Chloride Injection USP BD...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Chemistry A1c_3 CAL (Calibrator) for use on the ADVIA Chemistry...

The Issue: The ADVIA Chemistry Systems A1c_3 method may exhibit a percent bias of -9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Ellex iScience, Inc.

Recalled Item: iTRACK250A Canaloplasty Microcatheter Kit Recalled by Ellex iScience, Inc....

The Issue: One lot may not have been properly sealed, resulting in a non-sterile device.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Angiodynamics, Inc.

Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....

The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Angiodynamics, Inc.

Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....

The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Angiodynamics, Inc.

Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....

The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...

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

Class II — Potential Health HazardOngoing
DrugAugust 5, 2014· Zydus Pharmaceuticals USA Inc

Recalled Item: ZyGenerics ATENOLOL Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Superpotent Drug: A complaint was reported by a pharmacist who stated...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2014· Akorn, Inc.

Recalled Item: Rifampin for Injection USP Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurity/Degradation Specification; high out of specification result...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 5, 2014· Curbell Medical, Inc.

Recalled Item: CURBELL MEDICAL CareSense Wireless Advanced LCD Bed and Chair Monitor...

The Issue: The firm became aware of a potential problem that was initiated by a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2014· ICU Medical, Inc.

Recalled Item: CAP Change Kit w/MicroClave Clear Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...

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

Class II — Potential Health HazardOngoing