WECK IPN915193Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 24026704696820), received between Mar 29, 2022 and Nov 25, 2022 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Failure to Align” (2 reports).

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 25, 2022Failure to Align; Failure to Align

  IT WAS REPORTED THAT THE JAWS OF THE APPLIER WERE FOUND MISALIGNED BEFORE USE. THEREFORE, A NEW UNIT WAS USED INSTEAD.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15865129 ↗
• MalfunctionOct 28, 2022Failure to Align; Failure to Align

  IT WAS REPORTED THAT ON (B)(6) 2020, THE JAW WAS FOUND MISALIGNED DURING USING ON PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15694015 ↗
• MalfunctionMar 29, 2022Difficult or Delayed Separation; Difficult or Delayed Separation

  WHEN THE USER LIGATED A RENAL ARTERY WITH A CLIP DURING A LAPAROSCOPIC NEPHRECTOMY , THE CLIP GOT STUCK IN THE APPLIER. THE USER TOUCHED THE CLIP CAREFULLY WITH A FORCEPS, THEN THE CLIP LEFT THE APPLIER. THE CLIP DID NOT INVOLVE OTHER TISSUE AT LIGATION. ADDITIONAL INFORMATION: THE CLIP GOT STUCK IN THE APPLIER AFTER LIGATION, THEREFORE, WHEN THE CLIP LEFT THE APPLIER , LIGATION SUCCEEDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13939087 ↗