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 9001–9020 of 28,334 recalls
Recalled Item: BIO-RAD BioPlex 2200 Syphilis Total & RPR Calibrator Recalled by Bio-Rad...
The Issue: Due to two issues: 1) Customer complaints associated with greater than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIO-RAD BioPlex 2200 SYPH T PACK Syphilis Total Recalled by Bio-Rad...
The Issue: Due to two issues: 1) Customer complaints associated with greater than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Medical Linear Accelerator (EMLA) Recalled by Elekta, Inc. Due to...
The Issue: There is a risk that the Diode D1 in the Modulator can fail in a destructive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MEDRAD Twist & Go Disposable Syringe 150 mL with Recalled by Bayer...
The Issue: Labeling error: MEDRAD Mark 7 Arterion Injection System Syringes (ART 700...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Monaco - Product Usage: used to make treatment plans Recalled by...
The Issue: Contour changes can be saved on an unintended image set. In addition, these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Bio-Medicus Insertion Kits Recalled by Medtronic Perfusion Systems...
The Issue: There was a label mix-up between two model numbers resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCH Leg Positioning System Recalled by Innovative Orthopedic Technologies,...
The Issue: Due to the holes not being bored to the specific diameter, the locking pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIVE S 3.5x65 Recalled by Karl Storz Endoscopy Due to During a regular...
The Issue: During a regular requalification review, affected flexible intubation video...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foundation Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare Due...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IUD Insertion Pack Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenaculum Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endometrial Biopsy Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...
The Issue: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babylog VN500 Ventilator with Installed CO2 Measurement Option-intended for...
The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab (FLX) Recalled by Inpeco S.A. Due to The Firmware (FW) of the...
The Issue: The Firmware (FW) of the Automation System Interface Module to ADVIA Centaur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evita V500 Ventilator with Installed CO2 Measurement Option-Intended for the...
The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoHelical and TomoDirect plans in RayStation 6 Recalled by RAYSEARCH...
The Issue: If the dynamic jaw mode is used and an optimization is continued after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee Recalled by...
The Issue: Packaging may include screws that are not intended to be used with the 5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.