Caprosyn CC-975Recalls & reported problems
Covidien LP · Monofilament Absorbable Suture · Class 2 · Implant
All models of Caprosyn (45)
Data updated Oct 16, 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 10884523006049), received between Mar 23, 2020 and Mar 23, 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 16, 2026.
Most reported problems
Device problems
- Break1
- Detachment of Device or Device Component1
Patient problems
- No Consequences Or Impact To Patient1
- No Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 23, 2020Break; Break
ACCORDING TO THE REPORTER, DURING THE CAESARIAN SECTION PROCEDURE, THE DEVICE, NEEDLE TIP NOTED TO BE MISSING. THE SURGEON THEN FOUND THE MISSING TIP ON THE BACK TABLE AND PLACE IT IN A SPECIMEN CONTAINER FOR EVALUATION.
Patient problems: No Information
MAUDE report 9869759 ↗MalfunctionMar 23, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
ACCORDING TO THE REPORTER, DURING A CAESAREAN SECTION, A SUTURE SNAPPED OFF THE NEEDLE. NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9865297 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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