MUST MINI OC pre-bent transition Rod 03.75.897Recalls & reported problems
Medacta International SA · MUST MINI OC pre-bent transition Rod 75° Ø3.5/4x 200mm (ste) · 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 07630040723688), received between Apr 25, 2024 and Apr 25, 2024 — 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.
Reports received per month
Most reported problems
Device problems
- Positioning Failure1
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.
MalfunctionApr 25, 2024Positioning Failure; Positioning Failure
SPINAL FIXATION WAS PERFORMED AT OCCIPITAL BONE-C2/C3. THE SURGEON HAD DIFFICULTY SEATING MUST MINI OC PRE-BENT TRANSITION ROD INTO THE SCREW HEAD AT THE RIGHT SIDE OF C2 (TWO RODS WITH DIFFERENT ANGLES WERE TRIED). THE PART HE WAS TRYING TO SEAT WAS SILVER AND NOT GOLD, THEREFORE HE THOUGHT THE DIAMETER WAS 3MM, WHILE IT WAS MORE THAN 3MM AND SO COULD NOT BE PLACED INTO THE SCREW TULIP. A STRAIGHT ROD WAS USED TO COMPLETE THE SURGERY. ABOUT A 1-HOUR DELAY OVER A TOTAL SURGERY TIME OF 4 HOURS AND 30 MINUTES. THE SCREW WHICH WAS INSERTED AT THE C2 WAS REF:03.75.006,LOT:1923635 AND REF:03.75.006,LOT:2227122. NO PROBLEM ON THE LEFT SIDE OF C2.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19178565 ↗
Other Posterior Cervical Screw System devices
- INFINITY™ Occipitocervical Upper Thoracic System 3604026Medtronic Sofamor Danek, Inc. · Orthosis, cervical pedicle screw spinal fixation2 recalls1 report
- CONNECTOR 79-2002Orthofix US LLC · Posterior cervical screw system1 recall0 reports
- INFINITY™ Occipitocervical Upper Thoracic System 3604532Medtronic Sofamor Danek, Inc. · Orthosis, cervical pedicle screw spinal fixation1 recall0 reports
- INFINITY™ Occipitocervical Upper Thoracic System 3604024Medtronic Sofamor Danek, Inc. · Orthosis, cervical pedicle screw spinal fixation1 recall0 reports
- CONNECTOR 79-2003Orthofix US LLC · Posterior cervical screw system1 recall0 reports
- INFINITY™ Occipitocervical Upper Thoracic System 360PT4022Medtronic Sofamor Danek, Inc. · Orthosis, cervical pedicle screw spinal fixation1 recall0 reports
- OASYS 48551000Stryker Corporation · Orthosis, cervical pedicle screw spinal fixation45 reports
- SYMPHONY 1020-35-112Medos International Sàrl · Posterior cervical screw system6 deaths15 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