Medline DYNDTN0601ACSRecalls & reported problems
Medline Industries, Inc. · DEVICE, ACCESS, 20MM, MULTI-DOSE VIAL · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10884389191002), received between Sep 22, 2026 and Sep 30, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (3 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.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak3
- Loose or Intermittent Connection1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952171 ↗MalfunctionSep 23, 2026Fluid/Blood Leak
It was reported that ¿Access devices are defective and are causing vials to leak and therefore causing the studio to have to waste vials due to sterility concerns.¿
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872322 ↗MalfunctionSep 22, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50861965 ↗MalfunctionSep 22, 2026Fluid/Blood Leak
It was reported that "My bottles are dripping on my hands when I¿m drying vitamins up. Which if they¿re dripping out then it¿s a contamination."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50852766 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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