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. 2,491 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,491 in last 12 months

Showing 2088120900 of 28,355 recalls

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 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· 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 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· 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· 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 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 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 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 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· 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 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