Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,905 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,905 in last 12 months

Showing 2454124560 of 29,298 recalls

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 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· 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· 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 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 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 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 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 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 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· 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