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. 1,095 recalls have been distributed to Nevada in the last 12 months.
Showing 7081–7100 of 28,334 recalls
Recalled Item: RadiaLux Lighted Retractor (Pink) Recalled by Medtronic Navigation, Inc. Due...
The Issue: Defect in sterile pouch seal, incomplete seal, of lighted Retractors,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detect Covid-19 Test Product/Model Number: 21205 Recalled by Detect...
The Issue: There is an increased chance that the tests from affected lots may give...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS NEONATAL...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE PREP TRAY Recalled by MEDLINE...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE PERF. ASSOC. CUT DOWN TRAY...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE BREAST BIOPSY KIT Recalled by...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE ARM/MINOR DRAPE CSTM Recalled...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS L & D TRAY...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Trilogy 100 Ventilator Recalled by Philips Respironics, Inc. Due to...
The Issue: The replacement silicone sound abatement foam installed into some Trilogy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5 cm Large Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Identity Shoulder System Resection Planer 35mm Resection Planer Recalled by...
The Issue: Two planers were found to be unusable during sawbones shoulder training.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Thyroglobulin (US)- For in vitro diagnostic use with Recalled...
The Issue: Potential for Functional Sensitivity to not meet Instructions For Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Craniotome Recalled by The Anspach Effort, Inc. Due to Ball bearings...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobiCT-32 AIRO Mobile CT Scanner Recalled by Mobius Imaging, LLC Due to...
The Issue: Stryker received one report of an injury to an untrained user that occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5 cm Large Craniotome Attachment Use with XMax¿ Recalled by The Anspach...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Craniotome Recalled by The Anspach Effort, Inc. Due to Ball...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Trilogy 200 Ventilator Recalled by Philips Respironics, Inc. Due to...
The Issue: The replacement silicone sound abatement foam installed into some Trilogy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.