DTRAX Cervical Cage-B PD-31-200Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10852776006000), received between Feb 13, 2019 and Feb 13, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (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 18, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryFeb 13, 2019Adverse Event Without Identified Device or Use Problem; Migration; Adverse Event Without Identified Device or Use Problem; Migration

  ON (B)(6) 2019 PATIENT CONTACTED PMT AND REPORTED THAT ON (B)(6) 2017, HE UNDERWENT A POSTERIOR FUSION PROCEDURE AT C3-C4, AND C4-C5 LEVELS, WITH PMT CAGES. HE ALSO REPORTED A POSSIBLE TRAUMATIC INCIDENT POST PROCEDURE AS WELL AS FRACTURES AT C2, C5 AND C6, AS WELL AS AND 3 CAGE MIGRATIONS. CURRENTLY, ALMOST TWO YEARS POST PROCEDURE, PATIENT REPORTS PAIN, BOTH IN THE ARM AND NECK, INCONTINENCE, ARM NUMBNESS AND TINGLING, DIFFICULTY TO MOVE HIS RIGHT HAND AND TENDENCY TO LOSE CONSCIOUSNESS UPON ABRUPT NECK TURNING.

  Patient problems: Inadequate Pain Relief; Neck Pain

  MAUDE report 8338075 ↗