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Tritanium PL 48953080Recalls & 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 07613327117844), received between Apr 30, 2018 and Apr 30, 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.

  • MalfunctionApr 30, 2018Fracture

    THE PATIENT HAD A L5-S1 FUSION ON (B)(6) 17. THE PATIENT IMAGES LOOKED NORMAL ON SEVERAL FOLLOW UP APPOINTMENTS POST OP AND PATIENT APPEARED TO BE DOING WELL. ON HIS MOST RECENT FOLLOW-UP APPOINTMENT, THE SURGEON NOTICED THE CAGE WAS FRACTURED IN A POST OP X-RAY. THE PEDICLE SCREWS APPEAR NORMAL AND THE PATIENT IS NOT SYMPTOMATIC.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7474270 ↗

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Sources and updates

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