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. 2,510 recalls have been distributed to Nevada in the last 12 months.
Showing 27721–27740 of 28,334 recalls
Recalled Item: 4.5mm TI Multiloc Screw Length 28MM-Sterile Expiration: 04/29/2012 .019.028S...
The Issue: Two lots of 4.5mm multi-loc screws were recalled due to incorrect labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CYTO-STAT tetraCHROME CD45- FITC/CD56-RD1/CD19-ECD/CD3-PC5 Recalled by...
The Issue: The recall was initiated because Beckman Coulter has determined that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TetraCXP Software System Recalled by Beckman Coulter Inc. Due to The recall...
The Issue: The recall was initiated because Beckman Coulter has determined that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost Software Recalled by Philips Healthcare Inc. Due to...
The Issue: With Digital Diagnost (DIDI) R 2.0.2 a mirrored "R in a circle" is burnt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD GeneOhm MRSA ACP Assay Catalog #441637 Recalled by Becton Dickinson & Co....
The Issue: Leakage in Cepheid SmartCycler reaction tubes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage Cardiac Panel PN 97000HS Used for the quantitative Recalled by...
The Issue: Certain lots of the affected products may have significantly decreased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Software For use in the in-vitro quantitative...
The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Formula Shaver Handpiece (with buttons) Recalled by Stryker Endoscopy Due to...
The Issue: Stryker Endoscopy determined that there may not have been adequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympic Cool-Cap System is intended to provide treatment for neonatal...
The Issue: Olympic Cool-Cap Cooling Module's power supply failed during treatment. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva II with swivel cable Product Codes Recalled by...
The Issue: MultiDiagnost Eleva X--Ray system may have damage to System Cables from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to software...
The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Software For use in the in-vitro quantitative...
The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker MA204 Bed Model (FL25E) Beds are intended for medical Recalled by...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Rose Bed Model (FL14E) Beds are intended for medical Recalled by...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go Bed II+ Model FL28C Beds are intended for medical Recalled by Stryker...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GoBed+ . Model FL20E Beds are intended for medical purposes Recalled by...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go Bed II+ Model FL 28 Ex Beds are intended Recalled by Stryker Medical...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 9 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 13mm UPN Outer Box:...
The Issue: Difficulty in extending snare loop from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.