STERLING CUDA C9952ARecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854012574), received between Jul 15, 2022 and Jul 15, 2022 — 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.

• MalfunctionJul 15, 2022Break; Break

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE DEVICE C9952A, 2.9MM STERLING CUDA, 6 EA WAS BEING USED ON (B)(6) 2022 DURING A WRIST SCOPE PROCEDURE WHEN IT WAS REPORTED ¿SNAPPED IN HALF DURING WRIST SCOPE.¿ FURTHER ASSESSMENT FOUND THAT ¿THE SHAVER SNAPPED WHILE IN THE WRIST BUT WAS PICKED UP IMMEDIATELY. PATIENT WAS NOT INJURED." THE PROCEDURE WAS COMPLETED WITH A FEW MINUTES OF DELAY TO OPEN A NEW SHAVER. THERE WAS NO REPORTED INJURY, HOSPITALIZATION OR MEDICAL INTERVENTION FOR THE PATIENT. THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15026058 ↗