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Coated VICRYL J485HRecalls & 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 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705031040373), received between Aug 14, 2023 and Aug 14, 2023 — classified as 1 malfunction.

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

Patient problems

  • Hemorrhage/Blood Loss/Bleeding1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 14, 2023Break; Break

    IT WAS REPORTED AN ANIMAL UNDERWENT AN UNKNOWN VETERINARY PROCEDURE IN 2023 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE DISTRIBUTOR BY THE VETERINARY THAT DURING A SPAY AND MASS REMOVAL THE SUTURE BROKE WHILE TYING OFF OVARIES, DUE TO HIGH BLEEDING IT WAS A PROBLEM. SURGERY WAS EXTENDED TEN TO FIFTEEN MINUTES. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

    Patient problems: Hemorrhage/Blood Loss/Bleeding

    MAUDE report 17547401 ↗

Other SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID devices

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Sources and updates

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