Medline DYNJTS4301Recalls & reported problems
Medline Industries, Inc. · TRAY,LUMBAR PUNCTURE,PH ADULT,20X3.5 · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10080196741694), received between Sep 11, 2026 and Sep 11, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Tear, Rip or Hole in Device Packaging” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Tear, Rip or Hole in Device Packaging1
Patient problems
- Needle Stick/Puncture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 11, 2026Tear, Rip or Hole in Device Packaging
It was reported that the packaging has been arriving loose and at one point a staff member was poked by a needle packaged inside. This sample that I have shows a hole in the packaging.
Patient problems: Needle Stick/Puncture
MAUDE report 50734827 ↗
Other NEEDLE, SPINAL, SHORT TERM devices
- Portex 4924-25Icu Medical, Inc. · NEEDLE, SPINAL, SHORT TERM3 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.