Monterey ALRecalls & reported problems across all models
Stryker Corporation · 8 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
4 open recalls name at least one Monterey AL model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 4
We found 8 models of Monterey AL by Stryker Corporation in the FDA's device registry (GUDID). Together they are named in 6 adverse event reports in the FDA's MAUDE database, received between Mar 7, 2024 and Aug 29, 2025 — classified as 1 injury, 5 malfunctions.
The most frequently reported specific device problem is “Migration” (4 reports).
4 FDA recall records name at least one of these models by its device identifier, 4 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Monterey AL recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Feb 28, 2025Open, Classified
Potential for the gold unlock button to separate from the inserter.
Z-1491-2025 · Root cause: Device Design · Recall details · FDA record ↗
- Feb 28, 2025Open, Classified
Potential for the gold unlock button to separate from the inserter.
Z-1490-2025 · Root cause: Device Design · Recall details · FDA record ↗
- Feb 28, 2025Open, Classified
Potential for the gold unlock button to separate from the inserter.
Z-1489-2025 · Root cause: Device Design · Recall details · FDA record ↗
- Feb 28, 2025Open, Classified
Potential for the gold unlock button to separate from the inserter.
Z-1488-2025 · Root cause: Device Design · Recall details · FDA record ↗
Most reported Monterey AL problems
Device problems
- Migration4
- Difficult to Insert1
- Difficult to Remove1
- Insufficient Device Problem Information1
- Use of Device Problem1
Patient problems
- Pain4
- Hemorrhage/Blood Loss/Bleeding1
- No Clinical Signs, Symptoms or Conditions1
- Vascular Dissection1
Monterey AL models
8 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Monterey AL 48019100Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- Monterey AL 48019120Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- Monterey AL 48019130Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- Monterey AL 48019140Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- Monterey AL 480115020Intervertebral fusion device with integrated fixation, lumbar3 reports
- Monterey AL 480110531Intervertebral fusion device with bone graft, lumbar1 report
- Monterey AL 48019101Orthopedic manual surgical instrument1 report
- Monterey AL 48019108Orthopedic manual surgical instrument1 report
Recent Monterey AL adverse event reports
The 6 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryAug 29, 2025Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information
NO NEW INFORMATION.
Patient problems: Hemorrhage/Blood Loss/Bleeding; Vascular Dissection
MAUDE report 22923908 ↗MalfunctionFeb 27, 2025Difficult to Insert; Difficult to Remove; Difficult to Insert; Difficult to Remove
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21485293 ↗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 MONTEREY AL CAGE.
Patient problems: Pain
MAUDE report 18861805 ↗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 Stryker Corporation products
- RemB7 models · 3,073 reports
- Prime Series21 models · 1,548 reports · 2 recalls
- TARGET114 models · 1,077 reports
- ProCuity17 models · 368 reports · 13 recalls
- Spetzler-Malis20 models · 7 reports · 19 recalls
- SYNCHRO 28 models · 313 reports · 9 recalls
- Neptune E-SEP19 models · 412 reports · 7 recalls
- StrykeFlow4 models · 552 reports · 4 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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