AdvantageRib 323.1033Recalls & reported problems
Sig Medical Corp. · AdvantageRib Short Bridge and 23mm Locking Posts · 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 00854865007595), received between Aug 1, 2023 and Aug 1, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
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.
MalfunctionAug 1, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THE DURING THE IMPLANTATION PROCEDURE THAT THE POST SEPARATED FROM THE BRIDGE PLATE. THE SURGEON HAD THE POST TIGHTENED DOWN AND WENT TO DO ONE LAST CHECK TO SEE IF HE WAS SATISFIED WITH APPROXIMATION & STABILITY. UPON GENTLE PUSHING, HE REALIZED THE BRIDGE PLATE WAS NOT ATTACHED TO THE POST ANYMORE. PRODUCT WAS REMOVED FROM THE PATIENT. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17437805 ↗
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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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