Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,678 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,678 in last 12 months

Showing 2216122180 of 30,153 recalls

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
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 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 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 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 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 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 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 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 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 4, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue Module Measurement X2 Model: M3002A Recalled by Philips...

The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2016· C.R. Bard, Inc.

Recalled Item: Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters Recalled...

The Issue: Report by a customer of an open package seal.

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

Class III — Low RiskOngoing