L’DISQ® PD02Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08800015900003), received between Jul 31, 2018 and Jul 31, 2018 — 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.

• InjuryJul 31, 2018Break; Break

  THIS EVENT OCCURRED IN (B)(6). THE PATIENT HAD DISC DISEASE BETWEEN L4 AND L5 VERTEBRAE. THE PATIENT UNDERWENT DISC DECOMPRESSION PROCEDURE ON (B)(6) 2018. PART OF DEVICE(L'DISQ) WAS BROKEN OFF IN PROCESS OF THE PROCEDURE AND REMAINS IN THE BODY. PATIENT DOES NOT HAVE ANY PAIN . AND PATIENT DOES NOT WANT TO UNDERGO THE REMOVAL SURGERY. THEREFORE PART OF DEVICE WILL BE REMOVED FROM PATIENT'S BODY WHEN HE WANTS TO.

  Patient problems: Foreign Body In Patient

  MAUDE report 7734130 ↗