Medline Industries, Inc. DYNJ0713177Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942085088), received between Jul 18, 2018 and Jul 18, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

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 21, 2024Class IIOpen, Classified

   Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.

   Z-0779-2025 · 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.

• InjuryJul 18, 2018Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING A C-SPINE FUSION, THE SURGEON PULLED THE STRING AND THE NEURO SPONGE DETACHED INSIDE THE PATIENT'S NECK.

  Patient problems: Foreign Body In Patient

  MAUDE report 7700917 ↗