Surgipro ll VP-707-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 10884521038271), received between Oct 17, 2025 and Dec 25, 2025 — 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
- Detachment of Device or Device Component1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 25, 2025Break; Break
ACCORDING TO THE REPORTER, DURING AN OPEN REDUCTION AND ANCHORING OF THE LEFT TEMPOROMANDIBULAR JOINT UNDER GENERAL ANESTHESIA, WHILE THE DOCTOR WAS USING A SUTURE TO CLOSE THE SKIN, THE SUTURE NEEDLE BROKE. THE CIRCULATING NURSE AND INSTRUMENT NURSE IMMEDIATELY PERFORMED A DUAL-PERSON CHECK OF THE SUTURE NEEDLE¿S INTEGRITY AND CONFIRMED THAT NO BROKEN NEEDLE REMAINED INSIDE THE PATIENT. A NEW SUTURE WAS IMMEDIATELY REPLACED, AND THE SURGERY WAS COMPLETED IN COOPERATION WITH THE DOCTOR.
Patient problems: Insufficient Information
MAUDE report 23894379 ↗MalfunctionOct 17, 2025Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
IT WAS REPORTED THAT DURING A FLEXOR TENDON REPAIR, WHILE SUTURING OR PREPARING SUTURE AFTER PATIENT INCISION, THE SUTURE SNAPPED AND CAME OUT OF THE GAUGE OF THE NEEDLE. THE NEEDLE DID NOT FALL INTO THE PATIENT CAVITY. THE ISSUE WAS RESOLVED BY USING AN ALTERNATIVE SUTURE FROM ANOTHER MANUFACTURER. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23320895 ↗
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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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