Momentum UU052-30-0500Recalls & reported problems
Ulrich Medical Usa, Inc. · Screwdriver for locking screw, SR25,1/4"-square · Class 2
All models of Momentum (19)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00814386025072), received between Jul 15, 2020 and Jul 25, 2024 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Material Fragmentation” (5 reports).
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
- Material Fragmentation5
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Foreign Body In Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 25, 2024Material Fragmentation; Material Fragmentation
SCREWDRIVER BROKE AT THE TIP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19828034 ↗MalfunctionJun 13, 2024Material Fragmentation; Material Fragmentation
SCREWDRIVER BROKE AT THE TIP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19529094 ↗MalfunctionSep 7, 2022Material Fragmentation; Material Fragmentation
SCREWDRIVER TIP BROKE OFF DURING SURGERY. THERE WAS NO EFFECT ON THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15369822 ↗MalfunctionOct 30, 2020Material Fragmentation; Material Fragmentation
3 SCREWDRIVER TIPS BROKE OFF DURING SURGERY. THE TIPS WERE RECOVERED AND DISCARDED. THERE WAS NO EFFECT ON THE PATIENT BUT THIS MALFUNCTION HAS BEEN FILED AS AN MDR IN THE PAST. REPORT 3/3.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10766670 ↗MalfunctionJul 15, 2020Material Fragmentation; Material Fragmentation
A SCREWDRIVER TIP BROKE OFF DURING SURGERY DUE TO NOT USING THE TORQUE LIMITING HANDLE AND OVERTIGHTENING THE SCREW. THE SCREWDRIVER TIP WAS LODGED IN THE SCREW SO THE SCREW AND ROD HAD TO BE REMOVED TO RETRIEVE THE TIP.
Patient problems: Foreign Body In Patient
MAUDE report 10279658 ↗
Other Thoracolumbosacral Pedicle Screw System devices
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- Sequoia® 3301-1Zimmer Spine, Inc. · Orthosis, spinal pedicle fixation, for degenerative disc disease184 reports
- CD HORIZON® Spinal System 8590855Medtronic Sofamor Danek, Inc. · Orthosis, spinal pedicle fixation, for degenerative disc disease179 reports
- Vitality® 07.02011.001Biomet Spine LLC · Orthosis, spinal pedicle fixation, for degenerative disc disease3 recalls0 reports
- EXPEDIUM VERSE 199721001SMedos International Sàrl · Thoracolumbosacral pedicle screw system124 reports
- LineSider LS-N6SA7550Integrity Implants Inc. · Thoracolumbosacral Pedicle Screw System2 recalls1 report
- LineSider LS-N6SA6545Integrity Implants Inc. · Thoracolumbosacral Pedicle Screw System2 recalls0 reports
- EXPEDIUM VERSE 199721000SMedos International Sàrl · Thoracolumbosacral pedicle screw system97 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.
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