Monterey AL 480115020Recalls & reported problems
Stryker Corporation · Screw · Class 2 · Implant
All models of Monterey AL (8)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327422597), received between Mar 7, 2024 and Mar 7, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Migration” (3 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
- Migration3
Patient problems
- Pain3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 7, 2024Migration; Migration
IT WAS REPORTED THAT A MONTEREY AL CAGE AND THREE MONTEREY PLATE SCREWS HAVE MIGRATED ANTERIORLY APPROXIMATELY TWO-MONTHS POST-OPERATIVELY. REVISION SURGERY IS NOT CURRENTLY PLANNED BUT THE PATIENT HAS REPORTED EXPERIENCING PAIN. THIS REPORT CAPTURES THE THIRD OF THREE MONTEREY PLATE SCREWS.
Patient problems: Pain
MAUDE report 18861923 ↗MalfunctionMar 7, 2024Migration; Migration
IT WAS REPORTED THAT A MONTEREY AL CAGE AND THREE MONTEREY PLATE SCREWS HAVE MIGRATED ANTERIORLY APPROXIMATELY TWO-MONTHS POST-OPERATIVELY. REVISION SURGERY IS NOT CURRENTLY PLANNED BUT THE PATIENT HAS REPORTED EXPERIENCING PAIN. THIS REPORT CAPTURES THE FIRST OF THREE MONTEREY PLATE SCREWS.
Patient problems: Pain
MAUDE report 18861806 ↗MalfunctionMar 7, 2024Migration; Migration
IT WAS REPORTED THAT A MONTEREY AL CAGE AND THREE MONTEREY PLATE SCREWS HAVE MIGRATED ANTERIORLY APPROXIMATELY TWO-MONTHS POST-OPERATIVELY. REVISION SURGERY IS NOT CURRENTLY PLANNED BUT THE PATIENT HAS REPORTED EXPERIENCING PAIN. THIS REPORT CAPTURES THE SECOND OF THREE MONTEREY PLATE SCREWS.
Patient problems: Pain
MAUDE report 18861801 ↗
Other Intervertebral fusion device with integrated fixation, lumbar devices
- PIVOX™ Oblique Lateral Spinal System 2161001Medtronic Sofamor Danek, Inc. · Intervertebral fusion device with integrated fixation, lumbar182 reports
- IdentiTi 232-10-85-300Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall8 reports
- IdentiTi 232-10-85-250Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall5 reports
- IdentiTi 132-10-85-300Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall3 reports
- MectaLIF Anterior 03.30.301Medacta International SA · Intervertebral Fusion Device With Integrated Fixation, Lumbar1 recall2 reports
- IdentiTi 232-10-85-350Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall2 reports
- IdentiTi 232-11-90-350Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall1 report
- MectaLIF Anterior 03.30.302Medacta International SA · Intervertebral Fusion Device With Integrated Fixation, Lumbar1 recall1 report
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