Ecolab Hush Slush EquipmentRecalls & reported problems
Microtek Medical LLC · Hush Slush 2.0 Ecolab Slush & Warmer System · Class 1
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 50748426126731), received between Oct 22, 2024 and Oct 22, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Power Problem” (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.
Reports received per month
Most reported problems
Device problems
- Power Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 22, 2024Power Problem; Power Problem
IT WAS REPORTED THAT THE AUTO SLUSH IS NOT WORKING, IT DOES NOT MOVE WHEN POWERED ON. SLUSH POWER BUTTON IS CAUSING AN ELECTRIC SHOCK WHEN PRESSED. CUSTOMER WAS NOT INJURED FROM THE ELECTRICAL SHOCK. NO PATIENT INJURIES, INFECTIONS, OR COMPLICATIONS WERE REPORTED. .
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20506856 ↗
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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