Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 976 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
976 in last 12 months

Showing 36741–36760 of 52,570 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
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 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 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 Partial Knee System Phase 3 Tibial Template Left 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 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· Rymed Technologies, LLC

Recalled Item: InVision-Plus and InVision-Plus Junior Needleless IV Connector Recalled by...

The Issue: Potential for the female luer component of the InVision-Plus IV connector to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Rymed Technologies, LLC

Recalled Item: InVision-Plus CS Needleless IV Connector Recalled by Rymed Technologies, LLC...

The Issue: Potential for the female luer component of the InVision-Plus IV connector to...

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 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 Phase 3 Tibial Template Left 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 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 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 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