Sapphire Pulse Blower SFPULBRecalls & reported problems
Sizewise Rentals, L.L.C. · 120V Sapphire Pulse Blower Rev 3 P/N 61350002 / SFM Sapphire Pulse P/N 61356001 · 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 00845699000432), received between May 22, 2026 and May 22, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
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.
MalfunctionMay 22, 2026Insufficient Device Problem Information
THE BLOWER'S CONTROL PANEL IS EXHIBITING DISCOLORATION (TURNING BLACK) AND EMITTING A HOT ODOR. THE DEVICE REMAINED OPERATIONAL; HOWEVER, IT WAS NOTED TO FEEL HOT DURING USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25257538 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.