MUST Straight Cross Connector 03.56.403Recalls & reported problems
Medacta International SA · Straight Cross Connector 30mm · 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 07630040705844), received between Sep 16, 2019 and Sep 16, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Positioning Failure” (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
- Positioning Failure1
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 16, 2019Positioning Failure; Positioning Failure
SPINAL FIXATION PERFORMED AT T4-T8. THE SURGEON HAD A PLAN TO SET 3 CONNECTORS. THE SURGEON WAS NOT ABLE TO SET THE MUST STRAIGHT CROSS CONNECTOR AT T4-T5 BECAUSE BOTH HOOKS OF THE MUST STRAIGHT CROSS CONNECTOR CONTACTED TO THE FACET JOINT. OTHER 2 CONNECTORS WERE USED FOR OTHER INTERVERTEBRAL LEVEL. THEY CONTACTED TO THE FACET JOINT TOO, BUT THE SURGEON WAS ABLE TO SET THE MUST STRAIGHT CROSS CONNECTOR. 10 MINUTES OF DELAY REPORTED. TOTAL SURGERY TIME ABOUT 4 HOURS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9069328 ↗
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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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