Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,383 recalls have been distributed to Wyoming in the last 12 months.
Showing 24561–24580 of 27,462 recalls
Recalled Item: Portex¿ Saddleblock Tray with Drugs 26g Quincke Recalled by Smiths Medical...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Spinal Tray with Drugs 22g/25g Quincke Recalled by Smiths Medical...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Regional Anesthesia Tray with Drugs Recalled by Smiths Medical ASD,...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
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: Volcano s5/s5x/CORE Mobile 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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.