Halyard 92769Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10680651927696), received between Oct 2, 2018 and Oct 2, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Retraction Problem” (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.

• MalfunctionOct 2, 2018Retraction Problem; Retraction Problem

  IT WAS REPORTED THE GRASPERS WERE DIFFICULT TO REMOVE DURING THE PROCEDURE. ADDITIONAL INFORMATION RECEIVED 12-SEP-2018 STATED, THE RETRIEVAL BASKET WAS USED DURING A ENDOSCOPIC RETROGRADE CHOLANGIO-PANCREATOGRAPHY (ERCP) TO COLLECT A STONE IN COMMON BILE DUCT. THE PHYSICIAN WAS UNABLE TO REMOVE THE STONE, IT WAS PLAUSIBLE THE RETRIEVAL BASKET WAS STUCK IN THE STONE. AFTER SEVERAL ATTEMPTS THE WIRE WAS CUT FROM OUTSIDE THE PATIENT'S BODY AND THE SCOPE WAS WITHDRAWN. THE WIRE WAS REMOVED WHEN THE ERCP WAS PERFORMED ON (B)(6) 2018. THE PATIENT WAS AWAKE AND ALERT WITH MINIMUM PAIN AT THAT TIME.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7928180 ↗