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TRANSITION 152.612SRecalls & reported problems

Globus Medical, Inc. · TRANSITION 2-Level Implant, 60mm Rod, X-Lordotic, 22mm · Class 2

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 00849044023992), received between Feb 26, 2018 and Feb 26, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • MalfunctionFeb 26, 2018Break

    IT WAS REPORTED ON (B)(6) 2018 THAT A TRANSITION IMPLANT BROKE AND NEEDED TO BE REMOVED.

    Patient problems: Failure of Implant

    MAUDE report 7297610 ↗

Other POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.