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. 2,044 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,044 in last 12 months

Showing 51215140 of 28,334 recalls

Medical DeviceNovember 27, 2023· Mirion Technologies (Capintec), Inc.

Recalled Item: Captus 4000e Thyroid Uptake Systems- Intended to be used by Recalled by...

The Issue: Spring arm failure with Captus 4000e Thyroid Uptake Systems, can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2023· FUJIFILM Healthcare Americas Corporation

Recalled Item: The device is a mobile x-ray system designed to work Recalled by FUJIFILM...

The Issue: When the key switch is turned on, the exposure conditions are set to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2023· ACTIM OY

Recalled Item: Actim PROM dipstik Recalled by ACTIM OY Due to Interference testing has...

The Issue: Interference testing has shown that the presence of personal lubricants in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer running software version 1.16 or prior...

The Issue: There are potential performance issues found in the DxI 9000 Access...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Equinoxe Reverse Shoulder System Recalled by Exactech, Inc. Due to...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Vantage Mobile Bearing Tibial Inserts Recalled by Exactech, Inc....

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: AcuMatch Hip System Recalled by Exactech, Inc. Due to Exactech has received...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Equinoxe Shoulder System Recalled by Exactech, Inc. Due to Exactech...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Optetrak Logic Knee System Recalled by Exactech, Inc. Due to...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Alteon Hip XLE Liner Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Beckman Coulter, Inc.

Recalled Item: Access Ultrasensitive Insulin only used on the DxI 9000 Access Recalled by...

The Issue: There is an issue with the Access Ultrasensitive Insulin assay protocol file...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Truliant Knee System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Vantage Ankle System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Truliant Recalled by Exactech, Inc. Due to Exactech has received 3...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Novation Hip System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Optetrak Logic PS Knee System Recalled by Exactech, Inc. Due to...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Optetrak Knee System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Keystone Industries

Recalled Item: KeySplint Hard Clear - Indicated for the fabrication of orthodontic Recalled...

The Issue: Keyprint Keysplint Hard Clear 1 kg resin bottles were inadvertently packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Medtronic Inc.

Recalled Item: Protege GPS Self-Expanding Peripheral Stent System Recalled by Medtronic...

The Issue: Seal defects could compromise the ability of the product packaging to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit F30i Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing