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Tritanium PL 48954086Recalls & 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
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327117950), received between Jan 25, 2018 and Jan 25, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (1 report).

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

  • Fracture1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 25, 2018Fracture

    IT WAS REPORTED THAT A PATIENT HAD UNDERGONE AN L5/S1 SURGERY ON (B)(6) 2017. AT THE THREE MONTH POST-OPERATIVE APPOINTMENT, THE PHYSICIAN PERFORMED AN X-RAY AND NOTICED A BROKEN CAGE. THE PATIENT DID NOT REPORT ANY ACUTE PAIN ASSOCIATED WITH THE BROKEN CAGE. THERE WERE TWO IMPLANTED CAGES AND IT IS UNKNOWN WHICH OF THE CAGES IS BROKEN. THERE ARE NO REPORTS OF PATIENT INTERVENTION OR ADVERSE HEALTH CONSEQUENCES DUE TO THE BROKEN CAGE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7220327 ↗

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Sources and updates

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