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Coated VICRYL D7649Recalls & reported problems

Ethicon, LLC · Violet Braided (Polyglactin 910), Synthetic Absorbable Suture · Class 2 · Implant

All models of Coated VICRYL (350)

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 10705031028159), received between Oct 9, 2018 and Oct 9, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Misassembled” (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

  • Component Misassembled1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionOct 9, 2018Component Misassembled; Component Misassembled

    IT WAS REPORTED WHILE STOCKING THE DEVICE AT FACILITY ON AN UNKNOWN DATE, IT WAS NOTICED THAT THE PRODUCT LISTED ONLINE AND PRODUCT MASTER THE NEEDLE LISTED IS A TF-4 BUT THE PRODUCT CAME WITH A DIFFERENT CONFIGURATION: TF-5 NEEDLE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7946930 ↗

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Sources and updates

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