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 13961–13980 of 27,462 recalls
Recalled Item: Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra...
The Issue: Stability did not meet acceptance criteria for visual appearance during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec Heartmate 3 Sealed Outflow Graft with Bend Relief Recalled by...
The Issue: Outflow Graft leaking at the pump connection during the implantation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to...
The Issue: Outflow Graft leaking at the pump connection during the implantation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ally Bone Screw - Product Usage:Bone Screws are indicated for Recalled by...
The Issue: There may be dimensional manufacturing error that represents a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestilix 1600X Prestilix system is a fully integrated remote controlled...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to There has been a reported...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silhouette VR This fully integrated system offers intuitive controls with...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus XR/a The Proteus XR/a radiographic system offers the flexibility...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conformis iTotal Hip Replacement System: HBS-033-00xx-010101 Recalled by...
The Issue: Discrepancy of 3mm between the values displayed and approved by surgeons in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conformis iTotal Hip Replacement System: HBS-033-00xx-020101 Recalled by...
The Issue: Discrepancy of 3mm between the values displayed and approved by surgeons in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision 500D The Precision 500D R&F X-ray System is intended Recalled by...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Nail Clipper Concave Edge (67710) Recalled by Centurion Medical...
The Issue: Compromised seal on the sterile barrier pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Nail Nipper Recalled by Centurion Medical Products Corporation Due...
The Issue: Compromised seal on the sterile barrier pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Recalled...
The Issue: There is a potential of fracture, bending or shearing of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T7 Driver Solid AO (Part Number 110018541) Product Usage: The Recalled by...
The Issue: There is a potential of fracture, bending or shearing of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...
The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.