Medline Industries, Inc. ACC010309ARecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489998078), received between Jul 31, 2026 and Jul 31, 2026 — classified as 1 injury.

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

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.

Recalls naming this device

1. Nov 17, 2022Class IIOpen, Classified

   Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.

   Z-1072-2023 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

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

• InjuryJul 31, 2026Appropriate Device Problem Term/Code Not Available

  "The hospital had a patient code and the physician says that this Lactated Ringer Injection instead of the Sodium Chloride Injection caused them issues and they had to administer antibiotics."

  Patient problems: Insufficient Information

  MAUDE report 50102714 ↗