Alternate Blower ALTBRecalls & reported problems
Sizewise Rentals, L.L.C. · 120V Alternate Blower Rev 3 - 61355006 · Class 1
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 00845699000388), received between May 8, 2025 and Mar 9, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Electrical Overstress” (3 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.
Reports received per month
Most reported problems
Device problems
- Electrical Overstress3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 9, 2026Electrical Overstress
THE BLOWER WAS SENT TO AGILITI FOR REPAIR WITH THE REPORTED ISSUE OF POWER FAILURE. UPON OPENING THE DEVICE, AN AGILITI TECHNICIAN DISCOVERED INTERNAL BURN DAMAGE THAT CAUSED THE POWER FAILURE. BURN DAMAGE WAS OBSERVED ON THE SIDE PANEL ASSEMBLY, AND A MARK APPROXIMATELY 6 INCHES IN LENGTH WAS PRESENT ON THE INTERIOR SURFACE OF THE UNIT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24551961 ↗MalfunctionDec 30, 2025Electrical Overstress; Electrical Overstress
DEVICE WAS SENT IN FOR REPAIR AND UPON OPENING THE UNIT, THE TECHNICIAN FOUND BURN DAMAGE INTERNALLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23926672 ↗MalfunctionMay 8, 2025Electrical Overstress; Electrical Overstress
THE PUMP WAS SENT TO AGILITI'S CENTER OF EXCELLENCE (COE) FOR REPAIR OF A COMPONENT UNRELATED TO THIS ISSUE. DURING DEVICE INSPECTION, THE COE IDENTIFIED BURN MARKS INSIDE THE PUMP; NO EXTERIOR DAMAGE WAS FOUND. NO COMPLAINTS OR REPORTS REGARDING THIS ISSUE WERE FILED BY THE CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21985546 ↗
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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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