M.U.S.T. MINI Polyaxial Screw 03.75.209Recalls & reported problems
Medacta International SA · Cannulated Polyaxial Screw 4.0 x 28 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 07630030863875), received between Aug 27, 2025 and Aug 27, 2025 — classified as 1 injury.
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
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 27, 2025Adverse Event Without Identified Device or Use Problem; Migration; Adverse Event Without Identified Device or Use Problem; Migration
PRIMARY SURGERY WAS PERFORMED AT C2-C7 WITH MYSPINE CERVICAL GUIDE ON (B)(6). A CT SCAN TWO WEEKS AFTER SURGERY SHOWED NO PROBLEMS, BUT THREE WEEKS AFTER SURGERY, IT WAS DISCOVERED THAT THE SET SCREW AT THE RIGHT SIDE OF C7 HAD COME LOOSE. REVISION SURGERY WAS PERFORMED AFTER TWO MONTHS TO REPLACE WITH THE NEW SET SCREW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22902796 ↗
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- EXPEDIUM VIPER 196789480Depuy Spine, LLC · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
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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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