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. 2,538 recalls have been distributed to Nevada in the last 12 months.
Showing 21041–21060 of 28,334 recalls
Recalled Item: Zilver¿ 518RX Vascular Stent with Rapid Exchange Delivery System Recalled by...
The Issue: Manufacturing of the joint between the inner catheter and stylet of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus...
The Issue: Drager became aware of situations where the error message "Poti unplugged"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number:...
The Issue: Drager became aware of situations where the error message "Poti unplugged"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOLIS Microplate System Recalled by Bio-Rad Laboratories, Inc. Due to The...
The Issue: The error "Washer Reagent Clean Fluid" level low alarmed, which prompted the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Plaza Picture archiving and communication system. Software only. PACS...
The Issue: Siemens is releasing an updated software version to address several software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbiq infusion pump is a device used in a Recalled by Hospira Inc. Due...
The Issue: Potential for the Symbiq pole clamp assemblies to be missing the rubber stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The THERAKOS CELLEX Photopheresis System is a photoimmune therapy. Catalog...
The Issue: The Mallinckrodt (Therakos) post-market monitoring process detected an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Recalled by Baxter Corporation Englewood Due to All lots of RAPIDFILL...
The Issue: All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL- GBS Medium (Broth 3 ml Fill 13 x 100 mm Screw Cap Tube Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry Systems Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Concerto Basic Shower Trolley is intended for assisted hygiene care...
The Issue: Reports of the bolts connecting the stretcher to the hydraulic piston and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Increased U90-382 or...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hip Preservation System Signature Series PreBent Burs under the following...
The Issue: Metal shavings released from burs during use are due to contact between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL GBS Medium 20 ml in 100x15mm plate (Standard Petri Dish) Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARDEX I.C. Anti-Infective 2-Way 5cc Foley Catheter. Intended for urinary...
The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Aero-AL Impaction handle Catalog Number 48921007. Stryker Spine...
The Issue: Reported jamming of the impaction handle when assembled to the Inserter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARDEX I.C. Anti-Infective 2-Way 3cc Foley Catheter Recalled by C.R. Bard,...
The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.