Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,886 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,886 in last 12 months

Showing 2108121100 of 28,538 recalls

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 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 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· 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 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 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 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 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· 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 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 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 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