Recall StatusTerminated
Date Initiated2021-03-04
Date Terminated2024-07-12
Product Quantity15298 units WW: 9204 US; 6094 OUS
Reason for Recall
Potential for the device safety interlock to fail. The safety interlock prevents an empty single-use reload from being erroneously fired a second time. If the safety interlock fails and the empty single-use reload is fired a second time, the stapler may cut tissue but no staples will deploy from the empty reload, potentially resulting in a failed anastomosis, bleeding, tissue trauma, and the potential need to convert to an open procedure.
Firm Action
Covidien/Medtronic issued Urgent Medical Device Recall via Federal Express and/or certified mail beginning March 4, 2021, states reason for recall, health risk and action to take:
1. Please immediately quarantine and discontinue use of affected item codes with associated lot numbers listed on Attachment A.
2. Please return affected product as indicated below. All unused products from the affected item codes and associated lot numbers must be returned.
3. If you have distributed the Covidien Signia" small diameter curved tip intelligent reload listed on Attachment A, please promptly forward the information from this letter to those recipients.
4. Complete the Recalled Product Return Form even if you do not have inventory.
If you have any questions regarding this communication, please contact your Medtronic representative or Customer Service at 800-962-9888, option 2.
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide distribution - US Nationwide distribution and the countries of Austria, Belgium, Chile, China, Denmark, Finland,
France, Germany, Hong Kong, Ireland, Italy, Netherlands,
Norway, Poland, Portugal, Spain, Sweden, Switzerland,
United Kingdom.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.