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McKesson S8698GXRecalls & reported problems

Mckesson Medical-Surgical Inc. · SUTURE *5-0 POLYPRO 18 DSM13 · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

1 other recall cover devices cleared under the same FDA submission (K050947); 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Jun 24, 2026Open, Classified

    Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery.

    Z-2922-2026 · Root cause: Equipment maintenance · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K050947. One submission often covers many models, so check the product and lot details in each record.

  • Z-1180-2023 · Dec 2, 2022 · Open, Classified
    Surgipro II Monofilament Polypropylene Sutures Product Description Model Number VP-421X SURGIPRO*II 4-0 90CM V20 DA7P VP421X VP-435-X SURGIPRO II 4-0 90CM KV5 DA7P VP435X VP-541X S

Other Suture, Nonabsorbable, Synthetic, Polypropylene devices

All Suture, Nonabsorbable, Synthetic, Polypropylene devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.