INTERLINK 2C6921Recalls & reported problems
Baxter International Inc. · 3-Port Manifold with Check Valves, Large Bore Stopcock with Rotating Male Luer Lock Extension Set, 2 Injection Sites, Male Luer Lock Adapter with Retractable Collar · Class 2
All models of INTERLINK (17)
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 00085412035451), received between Nov 27, 2019 and Nov 27, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Disconnection” (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.
Most reported problems
Device problems
- Disconnection1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 27, 2019Disconnection; Disconnection
IT WAS REPORTED THAT AN UNSPECIFIED QUANTITY OF INTERLINK SYSTEM 3-PORT MANIFOLDS DISCONNECTED. THE EVENT WAS FURTHER REPORTED AS DURING A PROCEDURE THE "TUBING WAS CONNECTED TO EXTENSION SET AND DISCONNECTED DESPITE TIGHTENING BOTH ENDS UPON CONNECTING TO THE PATIENT". THE DISCONNECTION WAS OBSERVED "ON THE CONNECTION BETWEEN THE MANIFOLD AND THE PATIENT'S SIDE". THE TUBING FELL TO THE FLOOR. THE PATIENT WAS RECEIVING AN INFUSION OF UNSPECIFIED FLUIDS AND MEDICATIONS DUE TO PATIENT RECEIVING SPINAL/EPIDURAL. THE TUBING WAS CHANGED, AND THE PROCEDURE WAS COMPLETED WITHOUT FURTHER INCIDENTS. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9387078 ↗
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- IV Administration Set 490067B. Braun Medical Inc. · Stopcock, i.V. Set1 recall9 reports
- ICU Medical MC330174Icu Medical, Inc. · Stopcock, i.V. Set1 recall4 reports
- IV Administration Set 490432B. Braun Medical Inc. · Stopcock, i.V. Set1 recall3 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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