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 25321–25340 of 28,334 recalls
Recalled Item: Volcano s5i/s5ix/s5iz/CORE Intravascular Ultrasound Imaging and Pressure...
The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ComboMap Intravascular Flow and Pressure System Recalled by Volcano Corp Due...
The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)...
The Issue: The trial insertion instrument may disassemble during use due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Vantage Digital Panoramic System delivers high-value features standard...
The Issue: An error was identified in the Real Time Controller (RTC) firmware versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultima OPCAB System Recalled by Maquet Cardiovascular, LLC Due to MAQUET has...
The Issue: MAQUET has identified a potential issue with the ULTIMA OPCAB (part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDRAD¿ Stellant CT Injector System with Certegra Workstation Recalled by...
The Issue: The root cause investigation showed that the under-volume hazard can occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW VolumeShare 4 (ADVANTAGE WORKSTATION 4.3.) Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Absorber Original Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX 5.2 DB Server (running Oracle 10.1.0.4.0) Recalled by AGFA Corp. Due...
The Issue: System downtime and/or slow performance may result if software in use is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand: The ForeCYTE Breast Health Test Recalled by Atossa Genetics, Inc. Due...
The Issue: Atossa Genetics is recalling ForeCYTE Breast Health Test, Mammary Aspiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Individual units labeled in part: Recalled by Richard Wolf Medical...
The Issue: Richard Wolf Medical Instrument Corporation recieved a complaint stating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 200 Sterilizer (Single Door) Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD 200...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Brivo OEC715/785/865 C-Arm Recalled by GE Healthcare Beijing , Hangwei...
The Issue: GE is recalling certain lots of GE Brivo OEC715/785/865 C-Arm due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100NX Cassettes The STERRAD Sterilization System is a low Recalled...
The Issue: Advanced Sterilization Products (ASP) is recalling the three lots (13F049,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension LOCI TNI Troponin I Calibrator RC 621. The Recalled by...
The Issue: Siemens Dimension LOCI TNI Troponin I calibrator lot 3DD007 may demonstrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.