SeptAlign FG-0032Recalls & reported problems
Spirair, Inc. · Class 2 · Implant
- 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 00860011696308), received between Jan 28, 2025 and Jan 28, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
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.
MalfunctionJan 28, 2025Break; Break
DURING DELIVERY OF THE IMPLANT, IT WAS NOTED THAT A PORTION OF THE DELIVERY DEVICE TIP HAD BROKEN OFF INTO THE CARTILAGE. THE PIECE WAS EASILY RETRIEVED PRIOR TO COMPLETION OF THE PROCEDURE. THERE WAS NO ADVERSE EFFECT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21256330 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.