SYMPHONY 1020-84-600SRecalls & reported problems
Medos International Sàrl · SYMPHONY OCT SYSTEM DUAL DIAMETER ROD TITANIUM ALLOY diameter4.0 to 5.5X600mm · Class 2 · Implant
All models of SYMPHONY (113)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034523705), received between Oct 27, 2022 and Oct 27, 2022 — classified as 1 injury.
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
- Failure of Implant1
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 27, 2022Break; Break
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN JAPAN AS FOLLOWS: IT WAS REPORTED THAT AN UNKNOWN SURGERY (T9 TO S2) WAS PERFORMED ON (B)(6) 2021. IN (B)(6) 2022, IT WAS FOUND THAT THE ROD WAS BROKEN AT THE 5/S LEVEL ON THE RIGHT SIDE. ON (B)(6) 2022, A REVISION SURGERY WAS PERFORMED, AND THE ROD WAS REPLACED. REINFORCEMENT WAS ALSO PERFORMED. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT INVOLVES ONE SYMPHONY OCT SYSTEM DUAL DIAMETER ROD TITANIUM ALLOY DIAMETER4.0 TO 5.5X600MM. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: Failure of Implant; Unspecified Tissue Injury
MAUDE report 15679324 ↗
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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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