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MEDI-VAC 65651-920GRecalls & reported problems

Cardinal Health 200, LLC · Flex Advantage 1500cc with solidifer preloaded · Class 2

All models of MEDI-VAC (6)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 50885380153295), received between Mar 31, 2021 and Mar 31, 2021 — classified as 1 injury.

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

  • Exposure to Body Fluids1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 31, 2021Leak/Splash; Leak/Splash

    DURING THE SUBSTITUTION OF THE DEVICE, IN PARTICULAR WHILE OPERATOR WAS DEACTIVATING THE VACUUM REMOVING THE RED TUBE, THE BIOLOGICAL LIQUID WHICH WAS COLLECTED IN THE DEVICE, CAME OUT FROM THE RED TUBE AND HIT THE HEALTH CARE PROFESSIONAL IN ONE EYE. THE HCP WAS THEN MONITORED TO IDENTIFY THE HEALTH STATUS AND TESTED FOR POSSIBLE INFECTIONS. ON TOP OF THAT, INAIL WAS INFORMED (SUBMITTER'S COMMENT: INAIL IS THE NATIONAL AUTHORITY WHICH MONITORS INJURY ON THE WORKING PLACE).

    Patient problems: Exposure to Body Fluids

    MAUDE report 11598926 ↗

Other APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED devices

All APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED devices →

Sources and updates

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