Coated VICRYL J1036HRecalls & reported problems
Johnson & Johnson Medical GmbH · Coated Vicryl (Polyglactin 910) Suture, Violet Braided, Sterile, Synthetic Absorbable Suture · Class 2 · Implant
All models of Coated VICRYL (4)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10705031468641), received between Aug 9, 2024 and Aug 9, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (3 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
- Break3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 9, 2024Break; Break
IT WAS REPORTED THAT AN ANIMAL UNDERWENT AN OOPHORECTOMY ON (B)(6) 2024 AND SUTURE WAS USED TO LIGATE THE OVARIAN PEDICLE. BY TIGHTENING THE KNOT OF THE LIGATURE, THE SUTURE BROKE IN THE LENGTH OF THE STRAND, WITHOUT EXCESSIVE TENSION BEING EXERTED. ANOTHER DEVICE WAS USED TO CONTINUE THE PROCEDURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19951729 ↗MalfunctionAug 9, 2024Break; Break
IT WAS REPORTED THAT AN ANIMAL UNDERWENT AN OOPHORECTOMY ON (B)(6) 2024 AND SUTURE WAS USED TO LIGATE THE OVARIAN PEDICLE. BY TIGHTENING THE KNOT OF THE LIGATURE, THE SUTURE BROKE IN THE LENGTH OF THE STRAND, WITHOUT EXCESSIVE TENSION BEING EXERTED. ANOTHER DEVICE WAS USED TO CONTINUE THE PROCEDURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19951722 ↗MalfunctionAug 9, 2024Break; Break
IT WAS REPORTED THAT AN ANIMAL UNDERWENT AN OOPHORECTOMY ON (B)(6) 2024 AND SUTURE WAS USED TO LIGATE THE OVARIAN PEDICLE. BY TIGHTENING THE KNOT OF THE LIGATURE, THE SUTURE BROKE IN THE LENGTH OF THE STRAND, WITHOUT EXCESSIVE TENSION BEING EXERTED. ANOTHER DEVICE WAS USED TO CONTINUE THE PROCEDURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19951721 ↗
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- 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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