Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,921 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,921 in last 12 months

Showing 2438124400 of 29,154 recalls

Medical DeviceAugust 11, 2014· Primus Medical LLC

Recalled Item: Prime Care ¿ Transcend Mattress Recalled by Primus Medical LLC Due to The...

The Issue: The firm found that the top cover of the mattresses were delaminating.

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 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· 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· 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 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· 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· 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 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 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 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