EEA TRIEEAXL33XTRecalls & reported problems
Covidien LP · Black Circular Stapler with Tri-Staple Technology · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521593176), received between Feb 12, 2025 and Feb 12, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Failure to Anastomose1
- Tissue Breakdown1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 12, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
ACCORDING TO THE REPORTER, DURING A LEFT COLECTOMY, THE ANVIL DISENGAGED, BUT IT DID NOT FALL INTO PATIENT¿S CAVITY. THE SURGEON PER FORMED THE ANASTOMOSIS WITH MANUAL SUTURE.
Patient problems: Failure to Anastomose; Tissue Breakdown
MAUDE report 21368622 ↗
Other Stapler, surgical devices
- ECHELON ECH60SEthicon Endo-Surgery, LLC · Stapler, surgical1 death631 reports
- ECHELON ECH60LEthicon Endo-Surgery, LLC · Stapler, surgical467 reports
- ECHELON ECH45SEthicon Endo-Surgery, LLC · Stapler, surgical269 reports
- EEA TRIEEA28XTCovidien LP · Stapler, surgical220 reports
- ECHELON ECH60CEthicon Endo-Surgery, LLC · Stapler, surgical197 reports
- ECHELON ECH45CEthicon Endo-Surgery, LLC · Stapler, surgical138 reports
- EEA TRIEEA31XTCovidien LP · Stapler, surgical73 reports
- ETHICON EC3D60LEthicon Endo-Surgery, LLC · Stapler, surgical39 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.