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. 2,573 recalls have been distributed to Wyoming in the last 12 months.
Showing 1401–1420 of 27,462 recalls
Recalled Item: DreamStation Auto. Non-Continuous Ventilator. Recalled by Philips...
The Issue: Devices may possess a programming error resulting in an incorrect device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118 Recalled by...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Model Numbers (REF): (1) 781357 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10...
The Issue: Potential for temporary loss of imaging (X-ray) functionality due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 5300 Model Numbers (REF): (1) 782110 Recalled by Philips North America...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S Model Numbers (REF): (1) 781359 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Model Numbers (REF): (1) 781342 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Recalled by Philips North America Due to The potential for...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine SAM 350P Recalled by HeartSine Technologies Ltd Due to Due to a...
The Issue: Due to a component manufacturing issue, Automated External Defibrillator may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED Recalled by...
The Issue: Cannulated fenestrated polyaxial screws may be incorrectly labeled
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 3.0T Model Number (REF): 782145 Recalled by Philips...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade to MR 7700 Model Number (REF): 782130 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...
The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold...
The Issue: Device does not comply with the labeling requirements of international...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...
The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection needle Recalled by Spiggle & Theis Mt Gmbh Due to Affected product...
The Issue: Affected product show elevated cytotoxicity values. Use of affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number:...
The Issue: Siemens Healthcare Diagnostics is recalling the RAPIDPoint 500 Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breathing circuit set Recalled by Hamilton Medical AG Due to Ventilator...
The Issue: Ventilator coaxial breathing circuit may have a crack in blue tubing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 800 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 600 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.