Medline Industries, Inc. DYNJ42210DRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10195327375461), received between Jan 12, 2026 and Jan 12, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Air/Gas in Device” (2 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 12, 2026Break; Air/Gas in Device

  IT WAS REPORTED THAT ON (B)(6) 2025 "THE SYRINGE HANDLE BROKE AND SEEMED VERY FLIMSY" AND "MULTIPLE STAFF MEMBERS STATE THAT THE SYRINGES PULL A LOT OF AIR NO MATTER HOW YOU CLEAR IT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24041065 ↗
• MalfunctionJan 12, 2026Break; Crack; Air/Gas in Device

  IT WAS REPORTED THAT ON 12/09/2025 "THE SYRINGE HANDLE BROKE AND SEEMED VERY FLIMSY" AND "MULTIPLE STAFF MEMBERS STATE THAT THE SYRINGES PULL A LOT OF AIR NO MATTER HOW YOU CLEAR IT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24037586 ↗