INTERLINK/DUO-VENT 2C7551Recalls & reported problems
Baxter International Inc. · Nitroglycerin Set with DUO-VENT Spike, PVC Pump Segment, Injection Site, Male Luer Lock Adapter · Class 2
Data updated Oct 16, 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 00085412051840), received between Mar 30, 2022 and Mar 21, 2023 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (4 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 16, 2026.
Most reported problems
Device problems
- Fluid/Blood Leak4
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.
MalfunctionMar 21, 2023Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT A NITROGLYCERIN SET LEAKED FROM WHERE THE DRIP CHAMBER IS CONNECTED TO THE TUBING. THIS ISSUE WAS OBSERVED DURING PATIENT INFUSION WITH TAXOTERE. RE-MIXING OF A NEW BAG WAS PERFORMED. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16582950 ↗MalfunctionMay 4, 2022Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT A NITROGLYCERIN SET LEAKED. DURING A DOCETAXEL INFUSION, THE LEAK WAS OBSERVED "FROM THE CONNECTION BETWEEN THE DRIP CHAMBER AND THE IV TUBING". THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14281460 ↗MalfunctionApr 29, 2022Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT A NITROGLYCERIN SET LEAKED. WHILE HANGING A DOCETAXEL INFUSION, THE LEAK WAS OBSERVED "FROM THE CONNECTION BETWEEN THE DRIP CHAMBER AND THE IV TUBING". IT WAS NOT REPORTED IF THE SET WAS ATTACHED TO THE PATIENT AT THE TIME OF THE EVENT. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14251414 ↗MalfunctionMar 30, 2022Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED A NITROGLYCERIN SET WITH DUO-VENT SPIKE LEAKED. DURING A DOCETAXEL INFUSION, THE LEAK WAS OBSERVED "COMING FROM THE CHAMBER OF THE TUBING; SLOW DRIPS NOTED." THE INFUSION WAS STOPPED AND THE CHANGED OUT. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13956881 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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