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.
Showing 7241–7260 of 50,223 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Votrient (pazopanib) 200 mg tablets Recalled by Siegfried Barbera, SL Due to...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leica HistoCore PEGASUS (PROCESSOR Recalled by LEICA BIOSYSTEMS NUSSLOCH...
The Issue: There is an issue regarding poorly processed and/or damaged biopsy tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibration Serum Level 3 - IVD For use as a Recalled by Randox Laboratories...
The Issue: Target for Alkaline Phosphatase (ALP) for the AMP optimized to IFCC 37¿C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibration Serum Level 3 CAL2351 Recalled by Randox Laboratories Ltd. Due...
The Issue: CK Total in Calibration Serum Level 3, CAL2351, is running with a positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model:...
The Issue: Instructions for Use-User Deviations related to the reprocessing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (10 mm diameter) Model:...
The Issue: Instructions for Use-User Deviations related to the reprocessing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Dressing change kit Recalled by ROi CPS LLC Due to ROi CPS...
The Issue: ROi CPS manufactured and distributed medical convenience kits with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.