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. 2,481 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,481 in last 12 months

Showing 3618136200 of 51,202 recalls

DrugJanuary 5, 2016· Hospira Inc.

Recalled Item: Magnesium Sulfate in Water for Injection Recalled by Hospira Inc. Due to...

The Issue: Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 5, 2016· Mayne Pharma Usa

Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Mayne Pharma Usa Due to Lack...

The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness test

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Right Medial Tibial Trial Tray Size Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Right Medial Tibial Trial Tray Size Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Phase 3 Tibial Template Right Medial Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Right Medial Tibial Trial Tray Size Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Usage: Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Left Medial Tibial Trial Tray Size Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Phase 3 Tibial Template Right Medial Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Right Medial Tibial Trial Tray Size Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Left Medial Tibial Trial Tray Size Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage:...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Knee System Tibial Resector Body Tube & Guides Product Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Left Medial Tibial Trial Tray Size Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Right Medial Tibial Trial Tray Size Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Left Medial Tibial Trial Tray Size Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Biomet U.K., Ltd.

Recalled Item: Oxford Partial Knee System Phase 3 Tibial Template Right Medial Recalled by...

The Issue: Zimmer Biomet is conducting a medical device field action for various...

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

Class II — Potential Health HazardOngoing