Caprosyn CC-872Recalls & 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
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10884523006018), received between Sep 18, 2026 and Sep 21, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Break” (9 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break9
- Detachment of Device or Device Component9
Patient problems
- No Clinical Signs, Symptoms or Conditions9
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 21, 2026Break; Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50839194 ↗MalfunctionSep 21, 2026Break; Detachment of Device or Device Component
It was reported that prior to use of the device, the suture was broken. As soon as the suture packet was opened, the needle and suture were found to be separated, and the suture broke when touched. 9 boxes from the same batch had the same issue. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50839110 ↗MalfunctionSep 21, 2026Break; Detachment of Device or Device Component
It was reported that prior to use of the device, the suture was broken. As soon as the suture packet was opened, the needle and suture were found to be separated, and the suture broke when touched. 9 boxes from the same batch had the same issue. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50838962 ↗MalfunctionSep 21, 2026Break; Detachment of Device or Device Component
It was reported that prior to use of the device, the suture was broken. As soon as the suture packet was opened, the needle and suture were found to be separated, and the suture broke when touched. 9 boxes from the same batch had the same issue. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50838918 ↗MalfunctionSep 21, 2026Break; Detachment of Device or Device Component
It was reported that prior to use of the device, the suture was broken. As soon as the suture packet was opened, the needle and suture were found to be separated, and the suture broke when touched. 9 boxes from the same batch had the same issue. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50838842 ↗MalfunctionSep 21, 2026Break; Detachment of Device or Device Component
It was reported that prior to use of the device, the suture was broken. As soon as the suture packet was opened, the needle and suture were found to be separated, and the suture broke when touched. 9 boxes from the same batch had the same issue. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50838790 ↗MalfunctionSep 21, 2026Break; Detachment of Device or Device Component
It was reported that prior to use of the device, the suture was broken. As soon as the suture packet was opened, the needle and suture were found to be separated, and the suture broke when touched. 9 boxes from the same batch had the same issue. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50838711 ↗MalfunctionSep 21, 2026Break; Detachment of Device or Device Component
It was reported that prior to use of the device, the suture was broken. As soon as the suture packet was opened, the needle and suture were found to be separated, and the suture broke when touched. 9 boxes from the same batch had the same issue. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50838663 ↗MalfunctionSep 18, 2026Break; Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50821573 ↗
Other SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID devices
- Coated VICRYL VCP433HEthicon, LLC · SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 death1,093 reports
- Polysorb CL-915Covidien LP · SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID503 reports
- Coated VICRYL VCP493HEthicon, LLC · SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID435 reports
- V-Loc 180 VLOCL0316Covidien LP · SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 recall376 reports
- Coated VICRYL VCP345HEthicon, LLC · SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 death405 reports
- V-Loc 180 VLOCL0604Covidien LP · SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 recall328 reports
- V-Loc 180 VLOCA008LCovidien LP · SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 recall294 reports
- V-Loc 180 VLOCL0326Covidien LP · SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID330 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page