Surgipro ll VP-711-XRecalls & reported problems
Covidien LP · Monofilament Polypropylene · Class 2 · Implant
All models of Surgipro ll (70)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 10884521038387), received between Oct 4, 2017 and Oct 4, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 4, 2017Break; Break
ACCORDING TO THE REPORTER: OCCURRED DURING AN OPEN KIDNEY TRANSPLANT PROCEDURE. THE SUTURE WAS BEING USED FOR SEWING THE ARTERIAL AN ANATOMOSIS. DURING THE PULL UP OF THE SUTURE THROUGH THE TISSUE, THE SUTURE THREAD SNAPPED UNDER TENSION. IN ORDER TO RESOLVE THE ISSUE AND COMPLETE THE CASE, USED A DIFFERENT SUTURE WITHOUT ISSUE. THERE WAS NO PATIENT HARM. THE PATIENT OUTCOME IS ALIVE, NO INJURY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6914414 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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