Medline DYNDTN0512Recalls & reported problems
Medline Industries, Inc. · IV ADMIN SET, 60DRP, 2 NF PORTS, 96" · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884389714782), received between Sep 12, 2025 and Sep 22, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Device Contamination with Chemical or Other Material1
- Free or Unrestricted Flow1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
OtherSep 22, 2026Free or Unrestricted Flow
It was reported that "I used this tubing on a client, and the fluid did not stop infusing automatically. It continued to flow in even when the bag was empty, where it could potentially pull in air to the vein."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50854686 ↗MalfunctionSep 12, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT BD GRAVITY SET HAD FOREIGN MATTER. THE FOLLOWING INFORMATION WAS RECEIVED BY THE INITIAL REPORTER WITH THE FOLLOWING VERBATIM IT WAS REPORTED BY CUSTOMER THAT A BLACK SPECK IMBEDDED INTO PLASTIC OF BUERTROL OF IV GRAVITY SETS OBSERVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23038834 ↗
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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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