Centrolock® XSD01003Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03700879511740), received between Nov 13, 2020 and Nov 13, 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.

• InjuryNov 13, 2020Break; Entrapment of Device

  COMPLAINT RECEIVED ON 2020/10/19: "BROKEN DRIVER WHILE INSERTING A CENTROLOCK SCREW LAST WEEK." SCREW DRIVER TIP SHEERED OFF WHILST PLACING A 2.5 LOCKING SCREW. THE TIP WAS LEFT IN THE HEAD OF THE SCREW AND COULD NOT BE RETRIEVED. ADDITIONAL DATA ON 2020/10/20: THE BROKEN DRIVER TIP WAS FLUSH WITH THE SCREW, THEREFORE WAS NOT ABLE TO REMOVE THE DEBRIS & REMAINED IN THE PATIENT.

  Patient problems: Foreign Body In Patient

  MAUDE report 10836893 ↗