Product Recalls in Nevada

Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,522 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,522 in last 12 months

Showing 2334123360 of 28,334 recalls

Medical DeviceNovember 4, 2014· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...

The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2014· Novadaq Technologies, Inc.

Recalled Item: LUNA Chest Recalled by Novadaq Technologies, Inc. Due to Mislabeling

The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...

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

Class III — Low RiskOngoing
Medical DeviceNovember 4, 2014· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...

The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM PERMANENT CAUTERY HOOK Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Elekta, Inc.

Recalled Item: MOSAIQ Product Usage: MOSAIQ is an oncology information system used Recalled...

The Issue: A problem can exist in MOSAIQ resulting in the display of incorrect numeric...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM PERMANENT CAUTERY SPATULA Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM FENESTRATED BIPOLAR FORCEPS Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing