M.U.S.T. MINI Polyaxial Screw 03.75.106Recalls & reported problems
Medacta International SA · Polyaxial Screw 4.0 x 22 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 07630030863523), received between Sep 12, 2024 and Sep 12, 2024 — 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.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Movement Disorder1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 12, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PRIMARY SURGERY WAS PERFORMED AT C7-T2 WITH THE MYSPINE GUIDE ON (B)(6) 2024. WHEN THE SURGEON TRIED TO CREATE THE SCREW HOLE, HE WAS NOT ABLE TO SEAT THE MYSPINE GUIDE PROPERLY, SO HE CREATED THE SCREW HOLE AND INSERTED THE PEDICLE SCREW WITH THE FREEHAND. AFTER THE SURGERY, IT WAS DISCOVERED THE SYMPTOMS WHICH THE PATIENT UNABLE TO MOVE HIS FINGERS. CHECKING THE X-RAY, IT WAS FOUND THAT THE PEDICLE SCREW ON THE LEFT SIDE OF C7 WAS INTERFERING WITH THE ROOT OF T1, CAUSING NEUROLOGICAL SYMPTOMS. REVISION SURGERY WAS PERFORMED ON (B)(6) 2024. THE PEDICLE SCREW AT THE LEFT SIDE OF C7 WAS REMOVED, AND THE SYMPTOMS IMPROVED.
Patient problems: Movement Disorder
MAUDE report 20201054 ↗
Other Appliance, Fixation, Spinal Interlaminal devices
- EXPEDIUM 179702000Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL439 reports
- EXPEDIUM VERSE 199721001Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL227 reports
- XIA 3 48230000Stryker Corporation · APPLIANCE, FIXATION, SPINAL INTERLAMINAL193 reports
- VIPER 186715000Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 death167 reports
- NA 04.614.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL80 reports
- NA 04.615.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- EXPEDIUM VIPER 196789480Depuy Spine, LLC · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- Arsenal Deformity Spinal Fixation System 47127Alphatec Spine, Inc. · APPLIANCE, FIXATION, SPINAL INTERLAMINAL66 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page