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. 2,526 recalls have been distributed to Wyoming in the last 12 months.
Showing 12401–12420 of 27,462 recalls
Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CardioChek Starter Kit Recalled by Polymer Technology Systems,...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate 3 Mobile Power Unit Recalled by Thoratec Corp. Due to Excessive...
The Issue: Excessive static electricity can potentially cause unrecoverable power loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-se Fiber Optic Miller 2 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Mac 3 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to The G6...
The Issue: The G6 bellavista 1000 US ventilators may experience intermittent failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE Recalled by Greiner Bio-One North America, Inc. Due to The...
The Issue: The Vacuette 3.5mL Serup Sep Clot Activator Tubes may have been damaged at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620/650/650c A2 Product Usage: anesthesia systems are intended...
The Issue: GE Healthcare has become aware that there is a potential for a loose cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620/650/650c A1 Product Usage: anesthesia systems are intended...
The Issue: GE Healthcare has become aware that there is a potential for a loose cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to During a...
The Issue: During a routine inspection of a system, a crack on the C-arm holder was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1 . Recalled by...
The Issue: The abutment provided with the Implant System may be out of specification,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Recalled by Radiometer Medical ApS Due to The analyzers fail on...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX PLUS Recalled by Radiometer Medical ApS Due to The analyzers fail...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 630G System with SmartGuard Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 640G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 620G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.