Surgipro II VP-72-MXRecalls & reported problems
Covidien LP · Monofilament Polypropylene · Class 2 · Implant
All models of Surgipro II (73)
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 10884521038721), received between Feb 28, 2024 and Apr 3, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Break2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 3, 2024Break; Break
ACCORDING TO THE REPORTER, DURING A LAPAROSCOPIC CV (CARDIOVASCULAR) PROCEDURE, WHILE PERFORMING INTERRUPTED SUTURING TECHNIQUE, THE SUTURE THREAD BROKE IN THE MIDDLE WHILE TRYING TO TIE DOWN. A NEW SUTURE WAS USED TO RESOLVE THE ISSUE. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19032718 ↗MalfunctionFeb 28, 2024Break; Break
ACCORDING TO THE REPORTER, DURING THE CORONARY ARTERY BYPASS GRAFTING (CABG) PROCEDURE, AT THE TIME OF ANASTOMOSIS OF THE VESSEL VIA RUNNING SUTURING TECHNIQUE, THE TAIL OF THE SUTURE THAT WAS BEING USED TO TIE DOWN THE KNOT WAS BROKEN. A NEW SUTURE WAS OPENED TO RESOLVE THE ISSUE. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18797798 ↗
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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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