Alaris, VersaSafe 11499817Recalls & reported problems
BD Switzerland Sàrl · SE BLD 15DP 180MF 1VS DEHP FREE · Class 2
All models of Alaris, VersaSafe (10)
Data updated Oct 18, 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 10885403275265), received between Aug 19, 2020 and Aug 19, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Leak/Splash” (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.
Most reported problems
Device problems
- Leak/Splash1
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.
MalfunctionAug 19, 2020Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE SE BLD 15DP 180MF 1VS DEHP FREE EXPERIENCED LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: A LEAK WAS FOUND DURING THE TRANSFUSION AT THE JUNCTION AT THE INJECTION SITE FOR 2 TUBES OF THE SAME REFERENCE BUT FROM DIFFERENT BATCHES AND LAID BY 2 NURSES. DIFFERENT TO 2 DIFFERENT PATIENTS. THIS RESULTED IN LABILE BLOOD PRODUCT LOSS AND NECESSITATED A CHANGE OF TUBING.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10429206 ↗
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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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