Covidien LLC recalls EGIA45 CT AR MD THK REL, EGIA45CTAMT
Recalled Product
EGIA45 CT AR MD THK REL, EGIA45CTAMT
Hazard / Issue
The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.
Issued by
FDA
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