MUST Straight Cross Connector 03.56.402Recalls & reported problems
Medacta International SA · Straight Cross Connector 20mm · Class 2 · Implant
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 07630040705837), received between Sep 4, 2019 and Sep 4, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Difficult to Insert” (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
- Difficult to Insert1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 4, 2019Difficult to Insert; Difficult to Insert
THE SURGEON WAS NOT ABLE TO SET THE STRAIGHT CROSS CONNECTOR TO THE ROD, BECAUSE THE CONNECTION PART WITH ROD WAS NARROW, THICK AND THE STRAIGHT CROSS CONNECTOR WAS IN CONTACT WITH THE BONE AROUND THE ROD. THE SURGEON FINISHED THE SURGERY WITHOUT USING THE STRAIGHT CROSS CONNECTOR. DUE TO THIS EVENT, THE SURGERY WAS PROLONGED ABOUT 10 MINUTES.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8959079 ↗
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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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