Product Recalls in Louisiana

Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,730 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,730 in last 12 months

Showing 4368143700 of 51,202 recalls

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· Stryker Instruments Div. of Stryker Corporation

Recalled Item: The NAV3i Platform Power Box supplies the electrical components with...

The Issue: The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and...

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· Stryker Instruments Div. of Stryker Corporation

Recalled Item: The Stryker NAV3i Platform is a mobile cart platform consisting Recalled by...

The Issue: The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and...

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 12, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS (R) Chemistry Products Calibrator Kit 17 Recalled by Ortho-Clinical...

The Issue: Calibrator values assigned for the calibrator kit lots were released using a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2014· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system...

The Issue: Although the Flat Panel Detector (FPD) touch sensor is activated during use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS (R) Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...

The Issue: Calibrator values assigned for the calibrator kit lots were released using a...

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

Class II — Potential Health HazardOngoing
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: PYRIDOXINE HCL Recalled by John W Hollis Inc Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: Liver Derivative Complex for injection Recalled by John W Hollis Inc Due to...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: Papaverine HCl 30 mg Recalled by John W Hollis Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: Polidocanol 5% Solution for Injection Recalled by John W Hollis Inc Due to...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund