Medline Industries, Inc. DYNDV2013CRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10889942753505), received between Jun 13, 2023 and Sep 26, 2026 — classified as 1 injury, 3 malfunctions.

The most frequently reported specific device problem is “Connection Problem” (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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 26, 2026Connection Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50906481 ↗
• MalfunctionSep 21, 2026Material Deformation

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50848240 ↗
• InjuryJun 16, 2023Leak/Splash; Leak/Splash

  ACCORDING TO THE CUSTOMER, THE PATIENT WAS RECEIVING IV CONTRAST "VIA POWER INJECTOR" FOR AN "ORBITAL CT SCAN" WHEN THE "2ND PORT ON EXTENSION BEGAN TO SPEW CONTRAST".

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 17148706 ↗
• MalfunctionJun 13, 2023Material Integrity Problem; Material Integrity Problem

  EXTENSION SET LEAKED AFTER CONTRAST ADMINISTRATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17117347 ↗