Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,509 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,509 in last 12 months

Showing 2494124960 of 29,188 recalls

Medical DeviceMay 15, 2014· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific Chemistry Controls Level I and II LEVl: Amber Recalled by...

The Issue: The original mean assigned to the control too high, upon reassignment with...

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

Class III — Low RiskOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· Beckman Coulter Inc.

Recalled Item: Ultrasonic Transducer Kits For use with the Access Family of Recalled by...

The Issue: Beckman Coulter is initiating a field action because some Ultrasonic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan -Neg Breakpoint Combo Panel Type 34 Recalled by Beckman Coulter,...

The Issue: Siemens Healthcare Diagnostics has received complaints regarding panel...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· DeVilbiss Healthcare LLC

Recalled Item: DeVilbiss Model DV5x Series CPAP units. For use in treating Recalled by...

The Issue: A limited number of DV5x Series CPAP units were manufactured and shipped...

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

Class III — Low RiskOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing