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McKesson S663GXRecalls & reported problems

Mckesson Medical-Surgical Inc. · SUTURE *3-0 NYLON 18 DS24 · Class 2 · Implant

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

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10612479214443), received between May 1, 2020 and Feb 14, 2023 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (3 reports).

2 other recalls cover devices cleared under the same FDA submission (K900531); 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 18, 2026.

Most reported problems

Device problems

  • Break3

Patient problems

  • No Clinical Signs, Symptoms or Conditions2
  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionFeb 14, 2023Break; Break

    ACCORDING TO THE REPORTER, DURING AN OPEN BIOPSY PROCEDURE, AT THE TIME OF SUTURING VIA INTERRUPTED STITCH, THE SUTURE BROKE. ANOTHER SUTURE WAS USED TO RESOLVE THE ISSUE. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16376559 ↗
  • MalfunctionJun 29, 2022Break; Break

    ACCORDING TO THE REPORTER, DURING OPEN PROCEDURE OF WOUND CLOSURE, WHILE SUTURING, THE THREAD BROKE. TO RESOLVE THE ISSUE, ANOTHER SUTURE WAS USED. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14861054 ↗
  • MalfunctionMay 1, 2020Break; Break

    ACCORDING TO THE REPORTER, DURING AN OPEN PROCEDURE, THE SUTURE BROKE WHILE USING. ANOTHER SUTURE WAS OPENED AND COMPLETE THE CASE. THERE WAS NO PATIENT INJURY.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10016777 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K900531. One submission often covers many models, so check the product and lot details in each record.

  • Z-1174-2023 · Dec 2, 2022 · Open, Classified
    Monosof Monofilament Nylon sutures: Product Description CN-724 MONOSOF* 1 BLK 100CM GS25 X36 CN-791 MONOSOF* 2-0 BLK 100CM GCC90X36 CN-791-12 MONOSOF* 2-0 BLK 10
  • Z-1173-2023 · Dec 2, 2022 · Open, Classified
    Monofilament Nylon Suture (McKesson Branded) and Coated Braided Silk Suture (McKesson Branded) (1) S661GX 5-0 NYLON 18 DS18 (2)S683GX 4-0 SILK 18 DS18 (3) S683GX

Other Suture, Nonabsorbable, Synthetic, Polyamide devices

All Suture, Nonabsorbable, Synthetic, Polyamide devices →

Sources and updates

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