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. 2,595 recalls have been distributed to Nevada in the last 12 months.
Showing 16981–17000 of 28,334 recalls
Recalled Item: iBalance(R) UKA Recalled by Arthrex, Inc. Due to Arthrex part number...
The Issue: Arthrex part number AR-501-UFLC, size 3, batch 10123297, has the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Now computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosphere System with the following three components: HEM1 Advanced Monitor...
The Issue: Pre-procedural issues related to software defects
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Up computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm¿ O2 interventional fluoroscopic x-ray system Recalled by Medtronic...
The Issue: During servicing of certain internal components of the O-Arm O2 Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000) Recalled...
The Issue: Correction to update sterilizer software to prohibit the use of expired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magstim Rapid Therapy System consisting of: Rapid Mainframe Recalled by The...
The Issue: Users manuals not supplied with 4800-00T US Rapid Therapy System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Automated Immunoassay Analyzer performs three methods of...
The Issue: The firm has become aware of a potential issue that may affect the mixing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.zen model Interventional fluoroscopic x-ray system wireless...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis model Interventional fluoroscopic x-ray foot switch accessory...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous...
The Issue: A specific lot of the FlexFlowTM Venous Cannula, 200-200, is being recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Recalled...
The Issue: There have been reported incidents of fluid leaks at the luer connection....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIRO Mobile CT System Recalled by Mobius Imaging, LLC Due to If the...
The Issue: If the tilt-drive motor has an intermittent connection or broken encoder or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System...
The Issue: A faulty footswitch may result in unintended ultrasonic fragmentation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented...
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Recalled...
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer....
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.