Medline Industries, Inc. DYNJ69124ARecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10195327226640), received between Mar 22, 2023 and Mar 22, 2023 — classified as 3 injuries.

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMar 22, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER, THERE WAS AN INCIDENT WHEN USING THE SHOULDER SCOPE PACK, WHERE AFTER PLACEMENT WAS FOUND WITH THE SPINAL NEED "THE INNER STILET WAS STUCK."

  Patient problems: Needle Stick/Puncture

  MAUDE report 16591217 ↗
• InjuryMar 22, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER, THERE WAS AN INCIDENT WHEN USING THE SHOULDER SCOPE PACK, WHERE AFTER PLACEMENT WAS FOUND WITH THE SPINAL NEED "THE INNER STILET WAS STUCK".

  Patient problems: Needle Stick/Puncture

  MAUDE report 16590980 ↗
• InjuryMar 22, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER, THERE WAS AN INCIDENT WHEN USING THE SHOULDER SCOPE PACK, WHERE AFTER PLACEMENT WAS FOUND WITH THE SPINAL NEED "THE INNER STILET WAS STUCK".

  Patient problems: Needle Stick/Puncture

  MAUDE report 16590689 ↗