INTERLINK/CONTINU-FLO 2C6519Recalls & reported problems
Baxter Healthcare Corporation · CONTINU-FLO Solution Set, 2 Injection Sites, Male Luer Lock Adapter with Retractable Collar · Class 2
All models of INTERLINK/CONTINU-FLO (5)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00085412002194), received between Sep 21, 2018 and Nov 16, 2020 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Illegible Information” (2 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
- Illegible Information2
- No Flow1
Patient problems
- No Patient Involvement3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 16, 2020Illegible Information; Illegible Information
IT WAS REPORTED THAT THE SHIPPING LABEL OF THE UNKNOWN QUANTITY OF CONTINU-FLO SOLUTION SETS WAS PLACED OVER THE BARCODE AND PRODUCT DETAILS. THIS WAS IDENTIFIED PRIOR TO USE. THERE WAS NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Patient Involvement
MAUDE report 10845952 ↗MalfunctionNov 16, 2020Illegible Information; Illegible Information
IT WAS REPORTED THAT THE SHIPPING LABEL OF THE UNKNOWN QUANTITY OF CONTINU-FLO SOLUTION SETS WAS PLACED OVER THE BARCODE AND PRODUCT DETAILS. THIS WAS IDENTIFIED PRIOR TO USE. THERE WAS NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Patient Involvement
MAUDE report 10845488 ↗MalfunctionSep 21, 2018No Flow; No Flow
IT WAS REPORTED THAT FOUR UNITS OF CONTINU-FLO INTERLINK SETS WOULD NOT PRIME. THIS WAS IDENTIFIED PRIOR TO USE. THERE WAS NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Patient Involvement
MAUDE report 7899648 ↗
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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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