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 25481–25500 of 28,334 recalls
Recalled Item: Siemens RAD Fluoro Uro System (Ysio Recalled by Siemens Medical Solutions...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys...
The Issue: Based on a review of historic packaging validations, it was determined that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01 Recalled by H &...
The Issue: Medical device tubing used for endotracheal airway application may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captia Syphilis-G Test Kit Product Usage: This is an enzyme Recalled by...
The Issue: Trinity Biotech recalled Trinity Biotech Captia Syphilis IgG kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens...
The Issue: Reports relating to Biomet 3i's BellaTek Zirconia Dental Abutment fractures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex Femoral Arterial Cannula with Duraflo Coating...
The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayer brand A1CNow+ MULTI-TEST A1C SYSTEM TEST KITS (PART NUMBER...
The Issue: Test results from these lots may produce a high-bias reading (by up to 20%)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Mammo is a multi-modality Recalled by GE Healthcare It Due to There is...
The Issue: There is a potential safety issue with the 8.0.2 version software of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crocodile (size 3) are two-armed Recalled by Snug Seat Inc Due to The bolts,...
The Issue: The bolts, which secure the handles, on the Crocodile (size 3) could break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Title 2 Bone Screw Remover Instrument Recalled by Zimmer, Inc. Due to...
The Issue: Possibility of the weld to the quick-connect breaking when force is applied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Dispersion Aortic Perfusion Cannula with Duraflo...
The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Titanium Prosthesis Recalled by Medtronic Xomed, Inc. Due to One...
The Issue: One lot of the product was assembled using the Cam Head version of the same...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgicutt fully automated incision making device for bleeding time...
The Issue: ITC has determined that the blade in their Surgicutt with Blotting Paper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET Spine Recalled by Ebi, Llc Due to Polaris Translation Screw Failures...
The Issue: Polaris Translation Screw Failures were recently reported to Biomet Spine....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Urine Combo 5 Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Urine Combo 2 Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan plus Negative Combo 3 Sold outside of US only. Recalled by Siemens...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Combo 2 Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.