M.U.S.T. MINI Polyaxial Screw 03.75.207Recalls & reported problems
Medacta International SA · Cannulated Polyaxial Screw 4.0 x 24 Full thread + nut · Class 2 · Implant
Data updated Oct 18, 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 07630030863851), received between Jun 18, 2021 and Jun 18, 2021 — classified as 1 injury.
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
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Discomfort1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 18, 2021Appropriate Device Problem Term/Code Not Available
C3-C6 SURGERY PERFORMED ON (B)(6) 2021. AFTER THE SURGERY, THE PATIENT'S RIGHT LEG MOVEMENT WAS NO GOOD. THE SURGEON CHECKED WITH CT AND MRI IMAGES, BUT THE PEDICLE SCREW IMPLANTATION DID NOT INDICATE ANY PROBLEMS. THE SURGEON INFORMED (B)(6) EVENING THAT THE RIGHT LEG MOVEMENT DID NOT RECOVER, SO THE PATIENT MOVED TO ANOTHER HOSPITAL AND THE SURGEON REMOVED PEDICLE SCREWS IN ORDER TO PERFORM THE DECOMPRESSION THE SAME DAY OF PRIMARY SURGERY. THE REASON FOR THIS EVENT IS STILL UNKNOWN.
Patient problems: Discomfort
MAUDE report 12023463 ↗
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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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