Surgipro ll VP-976-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
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521039742), received between Apr 5, 2018 and Feb 2, 2020 — classified as 2 malfunctions.
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
- Detachment of Device or Device Component1
Patient problems
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 2, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
ACCORDING TO THE REPORTER, DURING AN OPEN PROCEDURE FOR ANEURISM, WHILE TAKING OUT THE DEVICE FROM THE PACKAGE WITH THE NEEDLE DRIVER. THE NEEDLE DISENGAGED FROM THE THREAD. IT HAPPENED WITH FOUR SUTURES FROM THE SAME LOT. THE EVENT OCCURRED DURING THE PROCEDURE, BUT THE DEVICE WAS NOT USED IN PATIENT. THE SURGEON USED ANOTHER DEVICE FROM ANOTHER LOT NUMBER TO RESOLVE THE CASE. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9656930 ↗MalfunctionApr 5, 2018Break; Break
ACCORDING TO THE REPORTER, DURING OPEN LIVER TRANSPLANT PROCEDURE, THE SURGEON BROKE 3 INDIVIDUAL SUTURES. THERE WAS NO PATIENT INJURY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7399803 ↗
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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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