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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Covidien EEA; STAPLER, SURGICAL

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Covidien EEA; STAPLER, SURGICAL Back to Search Results
Model Number TRIEEA28MT
Medical Device Problem Code Failure to Fire (2610)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/10/2026
Type of Reportable Event Malfunction
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Brand Name
EEA
Common Device Name
STAPLER, SURGICAL
Manufacturer (Section D)
Covidien
sabanetas industrial park
ponce PR 00716 -440
Manufacturer (Section G)
Covidien
sabanetas industrial park
ponce PR 00716 -440
Manufacturer Contact
mike bocchino
8200 coral sea st ne
mounds view, MN 55112--439
+1(800)646-4633
MDR Report Key50220096
Report Number2647580-2026-02340
Device Sequence Number21409856
Product Code GAG
UDI-Device Identifier10884521593022
UDI-Public(01)10884521593022(17)300731(10)P5H1065S(20)02
Combination Product (Y/N)N
Initial Reporter CountryCH
PMA/510(K) Number
K172361
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2026
Device Explanted Year2026
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,Company Representative
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 08/12/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model NumberTRIEEA28MT
Device Catalogue NumberTRIEEA28MT
Device Lot NumberP5H1065S
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/10/2026
Initial Report FDA Received Date08/12/2026
Date Device Manufactured08/20/2025
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient SexFemale
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