CD HORIZON® Spinal System 7041430Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885074030838), received between Jun 5, 2020 and Jun 5, 2020 — classified as 1 injury.

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

• InjuryJun 5, 2020Break; Break

  ADDITIONAL INFORMATION RECEIVED AS MEDICAL RECORDS AND REPORTED THAT: 2019 DEC 10: PATIENT STARTED TO ATTEND REHABILITATIVE THERAPY (B)(6) 2020: PATIENT VISITED FOR PHYSICAL THERAPY (B)(6) 2020: PATIENT VISITED FOR PHYSICAL THERAPY FOLLOW UP (B)(6) 2020: PATIENT VISITED FOR PHYSICAL THERAPY FOLLOW UP (B)(6) 2020: PATIENT VISITED FOR PHYSICAL THERAPY FOLLOW UP (B)(6) 2020: PATIENT VISITED FOR PHYSICAL THERAPY FOLLOW UP.

  Patient problems: Depression; Disability; Injury; Pain

  MAUDE report 10124594 ↗