Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,459 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,459 in last 12 months

Showing 2406124080 of 28,127 recalls

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
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· CooperSurgical, Inc.

Recalled Item: Cooper Surgical TAMPA CATHETER 5 French 33 cm. Intended for Recalled by...

The Issue: Sterility of the device may be compromised due to unsealed pouch

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