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. 1,065 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,065 in last 12 months

Showing 15001–15020 of 50,223 recalls

Medical DeviceAugust 6, 2021· Philips Ultrasound Inc

Recalled Item: Affiniti Diagnostic Ultrasound Systems: Software Versions 5.0 Recalled by...

The Issue: Due to a software defect that can intermittently cause the system to lock-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is Recalled by...

The Issue: Image acquisition failures and synchronization failure with the Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (IC-3893AE) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (IC-4593) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (IC-4593CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (IC-4593AE) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (IC-3893) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (IC-3893CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
DrugAugust 6, 2021· XELLIA PHARMACEUTICALS USA, LLC

Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...

The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2021· XELLIA PHARMACEUTICALS USA, LLC

Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...

The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2021· Hikma Pharmaceuticals USA Inc.

Recalled Item: Bleomycin for Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Labeling: Not elsewhere classified: Mislabeling

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugAugust 5, 2021· DuPont Nutrition USA, Inc

Recalled Item: Avicel Recalled by DuPont Nutrition USA, Inc Due to Out of specification...

The Issue: Out of specification results for conductivity.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund