MEDLINE INDUSTRIES, INC. DYNJT4553Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10198459458323), received between Jun 3, 2026 and Jun 4, 2026 — classified as 3 injuries.

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

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. Mar 19, 2026Class IIOpen, Classified

   During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

   Z-2038-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

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.

• InjuryJun 4, 2026Contamination

  ACCORDING TO THE FACILITY, INFECTIONS ACQUIRED WITH PATIENTS AFTER THE USE OF THE CUSTOM LAMINECTOMY PACKS.

  Patient problems: Unspecified Infection

  MAUDE report 25397745 ↗
• InjuryJun 3, 2026Contamination

  IT WAS REPORTED THAT, "INFECTIONS ACQUIRED WITH PATIENT AFTER THE USE OF THESE CUSTOM PACKS".

  Patient problems: Unspecified Infection

  MAUDE report 25382487 ↗
• InjuryJun 3, 2026Contamination

  "INFECTIONS ACQUIRED WITH PATIENT AFTER THE USE OF THESE CUSTOM PACKS".

  Patient problems: Unspecified Infection

  MAUDE report 25376887 ↗