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. 2,680 recalls have been distributed to Nevada in the last 12 months.
Showing 9421–9440 of 28,334 recalls
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Anatomic Shoulder System for the following Part Numbers: 1....
The Issue: Complaints have been received concerning the humeral stem failing to mate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MY01 Continuous Compartmental Pressure Monitor Recalled by MY01, INC. Due to...
The Issue: There is an incorrect version of the needle in the introducer part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KeyPrint Soft- bottle Recalled by Straumann USA LLC Due to Product label...
The Issue: Product label intended for the European community was distributed to the USA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUTTING ELECTRODE BIPO 24.5FR Recalled by Richard Wolf GmbH Due to Product...
The Issue: Product labeled as Cutting Electrode may contain BIVAP electrode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas infinity central lab running software version 3.01.03 through 3.02.08...
The Issue: Under specific circumstances created by the user, the cobas e flow test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST IMIPENEM RELEBACTAM. in vitro diagnostic Recalled by Biomerieux Inc...
The Issue: Major errors (Resistant result instead of Susceptible result) were observed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to There is the potential...
The Issue: There is the potential bacterial including Nontuberculous mycobacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EJM4011 Jamshidi Evolve" Bone Marrow Biopsy/Aspiration Needle with Specimen...
The Issue: Due to complaints received regarding incomplete/open packaging seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x...
The Issue: Due to complaints received regarding incomplete/open packaging seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.