Medline DYND2219Recalls & reported problems
Medline Industries, Inc. · ADAPTER,CATHETER/SYRINGE/LUER,STERILE · Class 1
- 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 10884389123430), received between Feb 10, 2026 and Feb 10, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Inaccurate Delivery” (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
- Inaccurate Delivery1
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.
MalfunctionFeb 10, 2026Inaccurate Delivery
ACCORDING TO THE CUSTOMER, "THE BLUE CATHETER ADAPTER DOES NOT ADEQUATELY FIT INTO THE FOLEY CATHETER LUMEN, RESULTING IN LEAKAGE AROUND THE CONNECTION BETWEEN THE CATHETER AND THE ADAPTER. THE MEDICATION WAS REPORTED TO LEAK OUT AROUND THE ADAPTER CONNECTION".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24308525 ↗
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- Cook G02327Cook Incorporated · CONNECTOR, CATHETER1 recall1 report
- CARDINAL HEALTH SU130-4601Cardinal Health 200, LLC · CONNECTOR, CATHETER1 recall0 reports
- Cook G02464Cook Incorporated · CONNECTOR, CATHETER1 recall0 reports
- Cook G02898Cook Incorporated · CONNECTOR, CATHETER1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.