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Sequoia® 3367-2Recalls & reported problems

Zimmer Spine, Inc. · 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 00889024335523), received between Nov 24, 2020 and Nov 24, 2020 — 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. How this data works · Data updated Oct 13, 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.

  • MalfunctionNov 24, 2020Fracture; Fracture

    THE PIECE OF THE HEX SOCKET AT THE TIP OF A DORSAL HEIGHT TOOL WAS FOUND BROKEN AFTER SURGERY. THERE WERE NO REPORTED SURGICAL IMPACTS.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10895997 ↗

Other Orthosis, spinal pedicle fixation, for degenerative disc disease 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.