Tritanium PL 48951126Recalls & reported problems
Stryker Corporation · Posterior Lumbar Cage · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327117622), received between Sep 2, 2024 and Sep 2, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Migration” (2 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Migration2
Patient problems
- Pain2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 2, 2024Migration; Migration
THE PATIENT UNDERWENT A REVISION SURGERY APPROXIMATELY ONE MONTH AFTER IMPLANTATION TO ADDRESS THE MIGRATION OF TWO TRITANIUM PL CAGES AT THE L4-L5 LEVEL. THE PATIENT REPORTED PAIN AND SUBSEQUENT IMAGING IDENTIFIED THE MIGRATED CAGES. THIS REPORT CAPTURES THE SECOND OF TWO MIGRATED TRITANIUM PL CAGE.
Patient problems: Pain
MAUDE report 20117337 ↗InjurySep 2, 2024Migration; Migration
THE PATIENT UNDERWENT A REVISION SURGERY APPROXIMATELY ONE MONTH AFTER IMPLANTATION TO ADDRESS THE MIGRATION OF TWO TRITANIUM PL CAGES AT THE L4-L5 LEVEL. THE PATIENT REPORTED PAIN AND SUBSEQUENT IMAGING IDENTIFIED THE MIGRATED CAGES. THIS REPORT CAPTURES THE FIRST OF TWO MIGRATED TRITANIUM PL CAGE.
Patient problems: Pain
MAUDE report 20117336 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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