Tritanium PL 48955076Recalls & reported problems
Stryker Corporation · Posterior Lumbar Cage · Class 2 · Implant
All models of Tritanium PL (45)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327118056), received between Jul 8, 2016 and Apr 3, 2018 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Break2
- Fracture2
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 3, 2018Fracture; Break; Fracture
IT WAS REPORTED THAT THE CAGE BROKE UPON INSERTION IN THE PATIENT. THE BROKEN PIECES WERE RETRIEVED AND A SECOND CAGE WAS USED TO COMPLETE THE CASE WITH A SURGICAL DELAY OF FIVE MINUTES. THERE ARE NO REPORTS OF ADVERSE HEALTH CONSEQUENCES TO THE PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7392121 ↗MalfunctionJul 8, 2016Break; Fracture; Fracture
IT WAS REPORTED THAT; 3 MINUTE SURGICAL DELAY TO GET & LOAD ANOTHER IMPLANT AFTER CAGE BROKE WHILE BEING LIGHTLY IMPACTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 5780203 ↗
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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 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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