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. 2,404 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,404 in last 12 months

Showing 2294122960 of 27,462 recalls

Medical DeviceAugust 12, 2014· Ethicon Endo-Surgery Inc

Recalled Item: PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model...

The Issue: The device may have a non-conforming component that may cause the device to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2014· Instradent USA, Inc.

Recalled Item: Neodent Titamax WS Cortical Implant ¿4.0 x 5 mm (Endosseous Recalled by...

The Issue: Product not approved for use in the US

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2014· ELITech Clinical Systems SAS

Recalled Item: ENVOY 500 AST Reagent Kit Recalled by ELITech Clinical Systems SAS Due to...

The Issue: Some users of ENVOY 500 AST Reagent Kit, 55255, for Envoy 500 systems are...

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

Class III — Low RiskOngoing
Medical DeviceAugust 11, 2014· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Magnesium RTU Reagent Recalled by Horiba Instruments, Inc dba...

The Issue: Horiba Medical is recalling the ABX PENTRA Magnesium RTU Reagent because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· CareFusion 203, Inc.

Recalled Item: CareFusion EnVe and ReVel Ventilators. The EnVe/ ReVel Ventilator is...

The Issue: CareFusion has identified a potential for damage to the power connector on...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 8, 2014· Baro-Therapies, Inc

Recalled Item: The Rejuvenator Chamber manufactured by Baro-Therapies Recalled by...

The Issue: The firm is distributing the Rejuvenator device without an approved 510(k).

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...

The Issue: Technical Support Bulletin issued in February 2013 did not mention...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...

The Issue: Technical Support Bulletin issued in February 2013 did not mention...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...

The Issue: Technical Support Bulletin issued in February 2013 did not mention...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...

The Issue: Technical Support Bulletin issued in February 2013 did not mention...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...

The Issue: Technical Support Bulletin issued in February 2013 did not mention...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...

The Issue: Technical Support Bulletin issued in February 2013 did not mention...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...

The Issue: Technical Support Bulletin issued in February 2013 did not mention...

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 UC 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 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