Surgipro ll VP-720-MXRecalls & 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521038615), received between Nov 27, 2018 and Nov 27, 2018 — classified as 1 injury.
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
- Difficult to Remove1
Patient problems
- Tissue Damage1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 27, 2018Break; Difficult to Remove; Break; Difficult to Remove
ACCORDING TO THE REPORTER, DURING AN OPEN FEM FEM BYPASS, WHILE SEWING GRAFT INTO ARTERY, THE SUTURE BROKE AND THE GRAFT CAME OUT OF ARTERY. BLOOD WAS LOST AT THAT TIME AND A NEW SUTURE WAS NEEDED TO REPAIR IT AND STOP BLOOD LOSS. THE SUTURE CAME UNRAVELED. AN UNANTICIPATED TISSUE LOSS RESULTED INTO THIS. TO COMPLETE THE PROCEDURE, THEY OPENED NEW SUTURES.
Patient problems: Tissue Damage
MAUDE report 8104832 ↗
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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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