Plain Gut SG-752Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10884521055995), received between Oct 11, 2024 and Oct 17, 2024 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

3 other recalls cover devices cleared under the same FDA submission (K142656, K885018); they may or may not involve this specific model.

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.

• MalfunctionOct 17, 2024Patient-Device Incompatibility; Patient-Device Incompatibility

  ACCORDING TO THE REPORTER, DURING A CARPAL TUNNEL OR TRIGGER FINGER RELEASE PROCEDURE, THE PATIENT HAD A MINOR REACTION TO THE SUTURE. THE DEVICE CAUSED RED AND RAISED AREAS, SOMETIMES BLISTERING.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 20470635 ↗
• MalfunctionOct 11, 2024Break; Break

  ACCORDING TO THE REPORTER, INTRA-OPERATIVELY OF A LIPOMA REMOVAL, DURING THE SKIN CLOSURE OR WHEN THE SURGEON HAS MADE THE KNOTS, THE SUTURE BROKE. THE ISSUE OCCURRED IN TWO SUTURES. ANOTHER KIND OF SUTURE WAS USED TO COMPLETE THE CASE. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20426168 ↗
• MalfunctionOct 11, 2024Break; Break

  ACCORDING TO THE REPORTER, INTRA-OPERATIVELY OF A LIPOMA REMOVAL, DURING THE SKIN CLOSURE OR WHEN THE SURGEON HAS MADE THE KNOTS, THE SUTURE BROKE. THE ISSUE OCCURRED IN TWO SUTURES. ANOTHER KIND OF SUTURE WAS USED TO COMPLETE THE CASE. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20426102 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K142656, K885018. One submission often covers many models, so check the product and lot details in each record.

• Z-1388-2023 · Mar 1, 2023 · Open, Classified
  Chromic Gut Absorbable Sutures, SURGIGUT* 0 CHR GS-25 90CM X36 (CG-904), SURGIGUT* 1 CHR GS-24 90CM X36 (CG-915), CHROMIC GUT 4-0 75CM V20 (GG-121), CHROMIC GUT 3-0 75CM V20 X36 (G
• Z-1389-2023 · Mar 1, 2023 · Open, Classified
  Mild Chromic Gut Absorbable Sutures, CH GUT 5-0 12 UD SS-14 SS-14 (G-1766-K), CHROMIC GUT 6-0 45CM HE-1 X12 (G-1780K)
• Z-1390-2023 · Mar 1, 2023 · Open, Classified
  Plain Gut Absorbable Sutures, PLAIN GUT 5/0 18 P-13 X12 (SG-5686), PLAIN GUT 4-0 18 UD SC-11 DA (SG828-2)