FIREBIRD 52-2140Recalls & reported problems
Orthofix US LLC · 140mm Rod · Class 2
Data updated Oct 16, 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 18257200016051), received between Mar 2, 2016 and Mar 2, 2016 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 2, 2016Break
INFORMATION PROVIDED STATES THAT PATIENT HAD L2-S1 FUSION IN 2013 USING (2) 140MM RODS. EXTENSION SURGERY WAS PERFORMED AFTER A FALL USING (2) 100MM RODS FROM L2-T12. THE (B)(6) 2015 X-RAYS REVEALED THAT ONE OF THE 140MM RODS HAD BROKE IN SITU. REVISION SURGERY WAS PERFORMED TO REMOVE ALL RODS AND REPLACED WITH (2) 450MM RODS.
Patient problems: No Code Available
MAUDE report 5475474 ↗
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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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