PRECICE Screw Tray STU1-001Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517001092), received between Aug 23, 2024 and Aug 23, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

• InjuryAug 23, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  ON (B)(6) 2024 A PATIENT UNDERWENT A POSTERIOR CERVICAL SPINAL FUSION PROCEDURE FROM C2 TO T3. DURING THE PROCEDURE THE IMPLANTED CONSTRUCT WAS CONNECTED TO AN EXISTING THORACO-SACRAL CONSTRUCT USING A TRANSITION ROD AND ROD-TO-ROD CONNECTORS. ON AN UNKNOWN DATE, THE PATIENT DEVELOPED POST-OPERATIVE DYSPHAGIA AND A REVISION PROCEDURE WAS SCHEDULED. ON (B)(6) 2024, DURING THE REVISION PROCEDURE, THE ROD-TO-ROD CONNECTOR ON THE LEFT C7 WAS FOUND TO HAVE SEPARATED FROM THE TRANSITION ROD. NO ADDITIONAL PATIENT IMPACT WAS REPORTED.

  Patient problems: Dysphagia/ Odynophagia

  MAUDE report 20050756 ↗