Integra® Jarit® 505232Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780158370), received between Apr 28, 2026 and Apr 28, 2026 — classified as 1 malfunction.

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 16, 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.

• MalfunctionApr 28, 2026Detachment of Device or Device Component

  THE FOLLOWING WAS REPORTED VIA MEDWATCH NUMBER (B)(4) THAT DURING A LAPAROSCOPIC OVARIAN CYSTECTOMY, THE COHEN ACORN CANNULA,2-1/8 CERV CONE,LG FOR 505-230 (505232) WAS "FOUND TO BE FUNCTIONAL; HOWEVER, PROPER ENGAGEMENT OF THE CONE TIP REQUIRES A 180-DEGREE TWIST FOR SECURE PLACEMENT. NO ONE NOTICED CONE MISSING FROM DEVICE UPON REMOVAL FROM USE. NO INJURY TO PATIENT, CONE PASSED SPONTANEOUSLY THROUGH VAGINA WHILE URINATING. THE CONE WAS NOT NOTICED TO BE MISSING IN THE OR. PHYSICIAN WAS MADE AWARE BY THE PATIENT AFTER DISCHARGE, WHO THEN ENSURED NO HARM OCCURRED. PATIENT RETURNED CONE TO PHYSICIAN¿S OFFICE DURING FOLLOW UP APPOINTMENT WHO INSPECTED CONE AND DETERMINED IT WAS INTACT. THE CONE WAS NOT RETURNED TO THE HOSPITAL." NO PATIENT INJURY OR DELAY REPORTED.

  Patient problems: Foreign Body In Patient

  MAUDE report 25023781 ↗