VICRYL RAPIDE VR844Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10705031134737), received between Feb 4, 2023 and Feb 4, 2023 — 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 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 4, 2023Break; Break

  IT WAS REPORTED THAT A PATIENT UNDERWENT A SKIN CLOSURE PROCEDURE ON (B)(6) 2023 AND SUTURE WAS USED. THE SUTURE BROKE WHEN TYING S KNOT DURING SKIN CLOSURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16301429 ↗
• MalfunctionFeb 4, 2023Break; Break

  IT WAS REPORTED THAT A PATIENT UNDERWENT A SKIN CLOSURE PROCEDURE ON (B)(6) 2023 AND SUTURE WAS USED. THE SUTURE BROKE TWO TIMES IN THE SAME CASE, WHEN TYING S KNOT DURING SKIN CLOSURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16301378 ↗
• MalfunctionFeb 4, 2023Break; Break

  IT WAS REPORTED THAT A PATIENT UNDERWENT A SKIN CLOSURE PROCEDURE ON (B)(6) 2023 AND SUTURE WAS USED. THE SUTURE BROKE TWO TIMES IN THE SAME CASE, WHEN TYING S KNOT DURING SKIN CLOSURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16301354 ↗