Medline Industries, Inc. DYNJ68844BRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10198459232428), received between Feb 27, 2026 and Feb 27, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (1 report).

2 FDA recall records name this device's identifier, 2 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-2027-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

2. Dec 12, 2025Class IIOpen, Classified

   Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.

   Z-1193-2026 · Root cause: Nonconforming Material/Component · 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.

• InjuryFeb 27, 2026Electrical /Electronic Property Problem; Melted

  ACCORDING TO THE FACILITY, ON (B)(6) 2026, DURING TRACHEAL SHAVE, THE PATIENT RECEIVED A BURN FROM THE GUARDED NEEDLE TIP BOVIE FROM THE SURGICAL PACK.

  Patient problems: Burn(s)

  MAUDE report 24472526 ↗