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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Covidien Surgical Tri-Staple 2.0; STAPLE, IMPLANTABLE

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Covidien Surgical Tri-Staple 2.0; STAPLE, IMPLANTABLE Back to Search Results
Model Number SIG30AVM
Medical Device Problem Code Failure to Fire (2610)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 07/29/2026
Type of Reportable Event Malfunction
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Brand Name
Tri-Staple 2.0
Common Device Name
STAPLE, IMPLANTABLE
Manufacturer (Section D)
Covidien Surgical
60 middletown ave
north haven CT 06473
Manufacturer (Section G)
Covidien Surgical
60 middletown ave
north haven CT 06473
Manufacturer Contact
mike bocchino
8200 coral sea st ne
mounds view, MN 55112--439
+1(800)646-4633
MDR Report Key50220789
Report Number1219930-2026-05032
Device Sequence Number10564652
Product Code GDW
UDI-Device Identifier10884521543669
UDI-Public(01)10884521543669(17)301231(10)N6A1261Y(20)03
Combination Product (Y/N)N
Initial Reporter CountryAS
PMA/510(K) Number
K160176
Number of Events Summarized1
Summary Report (Y/N)N
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 NumberSIG30AVM
Device Catalogue NumberSIG30AVM
Device Lot NumberN6A1261Y
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 07/29/2026
Initial Report FDA Received Date08/12/2026
Date Device Manufactured01/15/2026
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 SexUnknown
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