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. 2,503 recalls have been distributed to Wyoming in the last 12 months.
Showing 14741–14760 of 27,462 recalls
Recalled Item: Retractor System Elastic Stays (Part 3314-lG Recalled by CooperSurgical,...
The Issue: There is a possibility that the seal of the sterile pouch may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vereos PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Software Correction: Software errors that may result in incorrect 4D CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P...
The Issue: Small hole at the end of the syringe is impeding suction of liquid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm 400CE Recalled by Cincinnati Sub-Zero Products LLC, a Gentherm...
The Issue: Potential for membrane (control panel) switch errors leading to an inability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B850 Product Usage: Intended uses of...
The Issue: When multiple CARESCAPEMonitor B450 or B850 units are connected to the same...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colpo-Pneumo Occluder Recalled by CooperSurgical, Inc. Due to The seal of...
The Issue: The seal of the sterile pouch may be compromised, thereby increasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dash 5000 Patient Monitoring System is used to monitor physiologic Recalled...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solar 8000i Patient Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dash 3000 Patient Monitoring System is used to monitor physiologic Recalled...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dash 4000 Patient Monitoring System is used to monitor physiologic Recalled...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ashland(TM) Box Film Ball Cube II EBT3 Recalled by Accuray Incorporated Due...
The Issue: the Ball Cube II phantom calibration film was not manufactured within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solar 8000M Patient Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuoSaph Plus Endoscopic Vessel Harvesting System Recalled by Terumo...
The Issue: The system's IFU contains a list of generators that the have been deemed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solar 9500 Information Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB + Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...
The Issue: The product was shipped after its expiry date due to a system error. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mitek Screw and Washer Depth Gauge Recalled by DePuy Mitek, Inc., a Johnson...
The Issue: The device has an offset in the design that results in a reading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2 Recalled by...
The Issue: The reagent pack exhibits the potential for an increased frequency of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass ULTRA SYSTEM Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo 220/240V AC Recalled by Terumo Cardiovascular Systems Corporation Due...
The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.