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. 2,510 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,510 in last 12 months

Showing 1342113440 of 27,462 recalls

Medical DeviceMay 21, 2019· Medtronic Inc

Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling

The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· GE Healthcare, LLC

Recalled Item: LVivo EF app on Vscan Extend. Sold under the following Recalled by GE...

The Issue: Overestimation bias in automatically calculated ejection fraction (EF)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Medtronic Inc.

Recalled Item: Guardian Connect App CSS7200 iOS and Guardian Connect Transmitter GST4C...

The Issue: Customers using the firm's continuous glucose monitoring system application...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Opternative Inc

Recalled Item: The Visibly Online Vision Test which is part of Recalled by Opternative Inc...

The Issue: Lack of 510K clearance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product...

The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product...

The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Arrow International Inc

Recalled Item: Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip...

The Issue: Lidstock contains a labeling error. The lidstock shows the catheter cross...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· GE Healthcare, LLC

Recalled Item: Centricity PACS-IW with Universal Viewer version 5.0 Recalled by GE...

The Issue: There is a potential that one or more images or image series may be missing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer with PACS-IW foundation 6.0 Recalled by GE...

The Issue: There is a potential that one or more images or image series may be missing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 45 ARTICULATING XTRA THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 45MM MEDIUM/ THIC Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 30MM MEDIUM/ THICK RELOAD Recalled by Covidien LLC Due...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 45 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 30 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 60MM EXTRA THICK RELOA Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 CURVED TIP ART MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 ARTICULATING EXTRA THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 45MM EXTRA THICK RELOA Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing