CD HORIZON® Spinal System 99460040Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885074542553), received between Feb 13, 2017 and Feb 13, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Migration or Expulsion of Device” (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, 2017Migration or Expulsion of Device; Migration or Expulsion of Device

  IT WAS REPORTED THAT ON: (B)(6) 2015: THE PATIENT PRESENTED WITH A COMPLAINT OF BACK PAIN. ON (B)(6) 2015: THE PATIENT PRESENTED WITH PRE-OP DIAGNOSIS: LUMBAR DEGENERATIVE DISC (L3-L4) AND UNDERWENT THE FOLLOWING PROCEDURES: OBLIQUE APPROACH FOR ANTERIOR LUMBAR INTERBODY FUSION, L3-L4 WITH DISCECTOMY AND SUBSEQUENT PLACEMENT OF PEEK CAGE, 14 MM X 50 MM X 22 MM WITH 6 DEGREE LORDOSIS PACKED WITH PUTTY AND SUBSEQUENT INSTRUMENTATION WITH A 40 MM STRAIGHT PLATE. AS PER OP-NOTES, ¿..WE THEN WENT ON THE SIZE WITH TEMPLATES AND THEN SUBSEQUENTLY PLACED A PEEK CAGE 14 MM X 50 MM X 22 MM WITH 6 DEGREE LORDOSIS PACKED WITH PUTTY. THEN A 40 MM STRAIGHT PLATE WAS PLACED AFTER 5.5 X 35, TWO BOLTS WERE PLACED, ONE INTO THE L2 AND ONE AT L3 AND THEN 2 HEX NUTS WERE PLACED OVER THE DEVICE ANCHORING IN PLACE. WE THEN ALLOWED THE SOFT TISSUE FALLBACK TOGETHER AFTER REMOVAL OF OUR RETRACTOR.¿ THE PATIENT ALSO UNDERWENT THE FOLLOWING PROCEDURE: LATERAL LUMBAR INTERBODY FUSION WITH CAGE ALLOGRAFT AND ANTEROLATERAL PLATE L3-L4 FOR DEGENERATIVE DISC. AS PER OP-NOTES, ¿..WE THEN PREPARED FOR DISC REMOVAL AND FUSION. WE THEN USED A SERIES OF CURETTES TO DISSECT AWAY THE CARTILAGINOUS END PLATE AND FINAL

  Patient problems: No Code Available; Pain

  MAUDE report 6325049 ↗