Medline Industries, Inc. DYNJ901071KRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327504298), received between Apr 22, 2025 and Apr 22, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (1 report).

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.

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.

• InjuryApr 22, 2025Break; Break

  ACCORDING TO THE CUSTOMER, "DURING PUDENAL NERVE BLOCK, 25G HYPO NEEDLE WAS INSERTED POSTEROMEDIALLY TO THE ISCHIAL TUBEROSITY. UPON ASPIRATION, THE NEEDLE WAS NOTED TO BE BROKEN OFF AT THE CONNECTION WITH THE PLASTIC PORTION OF THE NEEDLE. ATTEMPTS TO RETRIEVE NEEDLE UNSUCCESSFUL."

  Patient problems: Foreign Body In Patient

  MAUDE report 21885089 ↗