MEDLINE DYND30331Recalls & reported problems
Medline Industries, Inc. · CONTAINER,SPECIMEN,OR STERILE, 4OZ · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 10080196032143), received between Sep 10, 2026 and Sep 10, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak1
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.
MalfunctionSep 10, 2026Fluid/Blood Leak
It was reported that "(b)(6) LOT 0332209A135 LEAKING."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50715546 ↗
Other CONTAINER, SPECIMEN, STERILE devices
- BD Vacutainer® Urine Analysis Preservative Tube 364992Becton, Dickinson And Company · CONTAINER, SPECIMEN, STERILE160 reports
- Medline Industries, Inc. DYNJ50241CMedline Industries, Inc. · CONTAINER, SPECIMEN, STERILE3 recalls0 reports
- BD Vacutainer® No Additive (Z) Tubes 366703Becton, Dickinson And Company · CONTAINER, SPECIMEN, STERILE143 reports
- Medline Industries, Inc. DYNJ63118AMedline Industries, Inc. · CONTAINER, SPECIMEN, STERILE2 recalls0 reports
- MyCareLink Smart™ 25000Medtronic, Inc. · CONTAINER, SPECIMEN, STERILE1 recall5 reports
- MyCareLink Smart™ 25000Medtronic, Inc. · CONTAINER, SPECIMEN, STERILE1 recall0 reports
- Para-Pak CLEAN 900312Meridian Bioscience, Inc. · Container, Specimen, Sterile1 recall0 reports
- Vacuette 450225Greiner Bio-One GmbH · CONTAINER, SPECIMEN, STERILE1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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