Medline Industries, Inc. DYNDV1934IRecalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10193489844955), received between Mar 11, 2024 and Mar 18, 2024 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Crack” (3 reports).

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 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 18, 2024Crack; Crack

  IT WAS REPORTED THAT THE PACK CONTAINED A CRACKED SYRINGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18927200 ↗
• MalfunctionMar 18, 2024Crack; Crack

  IT WAS REPORTED THAT THE PACK CONTAINED A CRACKED SYRINGE COMPONENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18927199 ↗
• MalfunctionMar 18, 2024Crack; Crack

  IT WAS REPORTED THAT THE PACK CONTAINED A CRACKED SYRINGE COMPONENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18927194 ↗
• MalfunctionMar 18, 2024Material Integrity Problem; Material Integrity Problem

  IT WAS REPORTED THAT THE PACK CONTAINED A BROKEN SYRINGE COMPONENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18927192 ↗
• MalfunctionMar 18, 2024Suction Problem; Suction Problem

  IT WAS REPORTED THAT A SYRINGE COMPONENT "WOULD NOT SUCTION."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18927143 ↗
• MalfunctionMar 18, 2024Break; Break

  IT WAS REPORTED THAT THE SYRINGE COMPONENT IN THE PACK HAD BROKEN "HANDLES."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18924175 ↗
• MalfunctionMar 18, 2024Break; Break

  IT WAS REPORTED THAT A BROKEN SYRINGE COMPONENT WAS WITHIN THE PACK.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18921437 ↗
• MalfunctionMar 11, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED THAT A SYRINGE COMPONENT WAS "NOT WORKING."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18881455 ↗