MEDLINE DYNDH1478Recalls & reported problems
Medline Industries, Inc. · LUMBAR PUNCTURE TRAY · 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 10193489193800), received between Jul 1, 2026 and Jul 1, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination” (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
- Contamination1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 1, 2026Contamination
FIBERS IN SPECIMEN TUBE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25678931 ↗
Other Lumbar puncture tray (adult & pediatric) devices
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- Safe-T 4301CSPCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall7 reports
- Safe-T 4306CWSPCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall7 reports
- N/A 4306CCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall4 reports
- N/A 4304CCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall1 report
- N/A 4306CWDFCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall0 reports
- MEDLINE DYNJTS07025Medline Industries, Inc. · Lumbar puncture tray (adult & pediatric)1 recall0 reports
- Safe-T 4306CSPCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.