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. 2,684 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,684 in last 12 months

Showing 80418060 of 50,223 recalls

Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· RoyalVibe Health Ltd.

Recalled Item: CellQuicken Analyzer (Smart-Watch and Software) Recalled by RoyalVibe Health...

The Issue: Ultrasound devices were not authorized, cleared, or approved by FDA, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: Citrine Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: 4500MD Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: API3200MD Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: Citrine QTRAP Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
DrugAugust 29, 2023· RB Health (US) LLC

Recalled Item: Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%) Recalled by...

The Issue: Labeling: Label Error on Declared Strength: The incorrect label on the back...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 29, 2023· CooperSurgical, Inc.

Recalled Item: Box as labeled: Regard Recalled by CooperSurgical, Inc. Due to Incorrect...

The Issue: Incorrect component descriptions within the "Contents" section on the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2023· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Arjo medical beds Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o. Due to...

The Issue: Unintended movement of bed wheels

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2023· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Arjo medical beds Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o. Due to...

The Issue: Unintended movement of bed wheels

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2023· Flower Orthopedics Corporation

Recalled Item: Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to...

The Issue: Device is breaking while in use, potential for patients to require a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2023· Becton Dickinson Infusion Therapy Systems Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to There is...

The Issue: There is the potential that the safety shield may not properly engage on IV...

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

Class II — Potential Health HazardOngoing
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's Organic Castor Oil Eye Drops Recalled by Dr. Berne's Whole...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's MSM MIST 15% Solution Recalled by Dr. Berne's Whole Health...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's MSM DROPS 5% Solution Recalled by Dr. Berne's Whole Health...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund