M.U.S.T. Cross Connectors 03.56.048Recalls & reported problems
Medacta International SA · MUST LINK 48-66 · Class 2
Data updated Oct 18, 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 07630030839795), received between Apr 25, 2019 and Apr 25, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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 18, 2026.
Most reported problems
Device problems
- Fracture1
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.
MalfunctionApr 25, 2019Fracture; Fracture
WHEN THE SURGEON TRIED TO LOOSEN THE CROSS CONNECTOR, THE LOCKING SCREW BROKE. THE SURGERY WAS FINISHED WITH THE BACK UP IMPLANT. DUE TO THIS EVENT THE SURGERY WAS PROLONGED ABOUT 10 MINUTES.
Patient problems: No Code Available
MAUDE report 8548840 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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