M.U.S.T. Pedicle Screw System 03.59.225Recalls & reported problems
Medacta International SA · MUST LT 25mm LONG - Pedicle Screw Ø6x45 Cann · Class 2 · Implant
All models of M.U.S.T. Pedicle Screw System (20)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07630971279544), received between Jul 7, 2021 and Jan 19, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Migration” (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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Migration1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 19, 2024Migration; Migration
THE PATIENT CAME IN FOR A POST-OP APPOINTMENT AND IT WAS OBSERVED THAT A SET SCREW HAD POPPED OUT. ABOUT 2 WEEKS AFTER THE PRIMARY SURGERY, THE SURGEON LOCKED DOWN THE ROD AND PUT IN A NEW SET SCREW. THE SURGERY WAS COMPLETED SUCCESSFULLY. TORQUE LIMITER USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18543707 ↗InjuryJul 7, 2021Adverse Event Without Identified Device or Use Problem
1 MONTH AFTER THE PRIMARY, THE PATIENT CAME IN REPORTING PAIN ON THE LEFT SIDE AND THE CAUSE OF THE PAIN IS UNKNOWN. THE SURGEON REMOVED THREE SCREWS FROM THE PATIENT'S LEFT SIDE AND DID NOT IMPLANT ANYTHING TO REPLACE THEM. THE SURGERY WAS COMPLETED SUCCESSFULLY.
Patient problems: Pain
MAUDE report 12127997 ↗
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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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