McKesson S687GRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10612479213118), received between Jan 15, 2026 and Jan 15, 2026 — classified as 3 malfunctions.

3 other recalls cover devices cleared under the same FDA submission (K142656); 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.

• MalfunctionJan 15, 2026Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE REPORTER, ON (B)(6) 2025, 5 DAYS AFTER THE LOWER BLEPHAROPLASTY, THE PATIENT EYES WERE VERY SWOLLEN. IT WAS OBSERVED THAT THE BODY WAS REJECTING THE SUTURE CAUSING THE EYELID TO SWELL, BLISTER, WATER AND SAG. THE PATIENT WAS PRESCRIBED BY ANTIBIOTIC/STEROID EYE DROP.

  Patient problems: Swelling/ Edema

  MAUDE report 24085103 ↗
• MalfunctionJan 15, 2026Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE REPORTER, ON (B)(6) 2025, 5 DAYS AFTER THE LOWER BLEPHAROPLASTY, THE PATIENT HAD VERY SWOLLEN EYES, IT WAS OBSERVED THAT THE BODY WAS REJECTING THE SUTURE CAUSING THE EYELID TO SWELL, BLISTER, WATER AND SAG. THE PATIENT WAS PRESCRIBED BY ANTIBIOTIC AND STEROID EYE DROP.

  Patient problems: Swelling/ Edema

  MAUDE report 24085069 ↗
• MalfunctionJan 15, 2026Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE REPORTER, ON (B)(6) 2025, 5 DAYS AFTER THE LOWER BLEPHAROPLASTY PROCEDURE, THE PATIENT'S EYES WERE VERY SWOLLEN. IT WAS OBSERVED THAT THE BODY WAS REJECTING THE SUTURE CAUSING THE EYELID TO SWELL, BLISTER, WATER AND SAG. THE PATIENT WAS GIVEN STEROID AND ANTIBIOTIC DROPS WHICH APPEAR TO BE HELPING BUT VERY SLOWLY.

  Patient problems: Swelling/ Edema

  MAUDE report 24084985 ↗

Recalls under the same FDA submission

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

• 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)
• 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)