CF back plate 143334ACRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046768072756), received between Aug 1, 2025 and Aug 1, 2025 — classified as 1 malfunction.

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. How this data works · Data updated Oct 13, 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.

• MalfunctionAug 1, 2025Break; Unintended Movement; Break; Unintended Movement

  GETINGE BECAME AWARE OF AN ISSUE INVOLVING ONE OF OUR ACCESSORIES ¿ 143334AC - CARBON- FIBRE BACK PLATE FOR SHOULDER. ACCORDING TO THE REPORT, THE ACCESSORY BROKE AT THE END OF THE SURGERY AND FELL TO THE FLOOR. THE INCIDENT OCCURRED WHILE THE PATIENT WAS STILL SEDATED ON THE OPERATING TABLE. THE FALL CAUSED EXTUBATION, AS THE TUBE HOLDER WAS ATTACHED TO THE ACCESSORY. THE PATIENT WAS ASSESSED BY BOTH THE SURGEON AND THE ANESTHESIOLOGIST, WITH NO INJURIES REPORTED. HOWEVER, WE DECIDED TO REPORT THIS ISSUE DUE TO THE POTENTIAL RISK OF SERIOUS INJURY IF A SIMILAR INCIDENT, NAMELY ACCESSORY BREAKAGE LEADING TO THE PATIENT'S EXTUBATION, WAS TO REOCCUR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22684775 ↗