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Plain Gut 6-0 18" PC-1 Conventional Cutting 3/8C 13mm B1916NRecalls & reported problems

Surgical Specialties México, S. de R.L. de C.V. · Plain Gut 6-0 18" PC-1 Conventional Cutting 3/8C 13mm · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00848782004751), received between May 24, 2022 and May 24, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Use of Device Problem” (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 18, 2026.

Most reported problems

Device problems

  • Use of Device Problem1

Patient problems

  • Wound Dehiscence1

Recent adverse event reports

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

  • InjuryMay 24, 2022Use of Device Problem

    ASSISTANT STATED THAT DURING UPPER LID BLEPHAROPLASTY PROCEDURES THE DOCTOR FOUND THAT THE SUTURES WERE NOT DISSOLVING AS THEY NORMALLY WOULD. THIS LEAD TO ONE PATIENT HAVING A WOUND THAT ENDED UP OPENING AND THREE OTHER PATIENTS BUMPS. THE DOCTOR HAS USED THESE TYPE BEFORE WITH NO ISSUES. THE TECHNIQUE USED OR A PHOTO WAS NOT ABLE TO BE PROVIDED. THIS HAPPENED WITHIN THE LAST 2-3 WEEKS AND IT HAPPENED WITH PATIENTS IN THEIR MIDDLE 50''S EARLY 60''S. THE DOCTOR HAD SEEN TWO PATIENTS YESTERDAY AND THEY WERE DOING FINE.

    Patient problems: Wound Dehiscence

    MAUDE report 14490442 ↗

Other SUTURE, ABSORBABLE, NATURAL devices

All SUTURE, ABSORBABLE, NATURAL devices →

Sources and updates

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