Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 943 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
943 in last 12 months

Showing 42481–42500 of 49,990 recalls

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· 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 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· 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· 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· 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