Medline Industries, Inc. DYNJ03013Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10080196973828), received between May 6, 2024 and May 15, 2024 — classified as 2 injuries.

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMay 15, 2024Break; Break

  ACCORDING TO THE CUSTOMER, ON (B)(6) 2024 THE FORCEPS BROKE OFF INSIDE THE PATIENT DURING "NORMAL USE" AND THE PIECE WAS "EASILY RETRIEVED".

  Patient problems: Foreign Body In Patient

  MAUDE report 19326060 ↗
• InjuryMay 6, 2024Insufficient Device Problem Information; Insufficient Device Problem Information

  ACCORDING TO THE CUSTOMER, "LAST WEEK THE NEEDLE HOLDER BROKE AND A PHYSICIAN WAS STUCK WITH A NEEDLE. THE PHYSICIAN HAD TO BE SEEN IN THE ER FOR BLOOD WORK AND STARTED TREATMENT FOR ANTI-AIDS RETROVIRAL (TRIPLE THERAPY). THE STICK HAPPENED AFTER THE NEEDLE WAS USED ON THE PATIENT".

  Patient problems: Insufficient Information

  MAUDE report 19248202 ↗