Fluent® INSTRUMENT FLUENT 780 BASE UNITRecalls & reported problems
Tecan Schweiz AG · configurable liquid handling workstation · 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 07640137481117), received between Aug 7, 2024 and Aug 7, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Fell” (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
- Device Fell1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 7, 2024Device Fell; Device Fell
CUSTOMER REPORTED FLUENT 780 FRONT SHIELD DOES NOT REMAIN OPEN AND FALLS FROM AN OPEN POSITION. THE CUSTOMER CONFIRMED NO INJURIES OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Patient Involvement
MAUDE report 19928256 ↗
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- STAR COMPL. WITH ACCESS. 185080Hamilton Bonaduz AG · Station, Pipetting And Diluting, For Clinical Use2 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.