Integra® Jarit® 605152Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Tenaculum Forceps, 13-1/2", Slide Lock, double action insulated, 5mm · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780146650), received between Jun 4, 2024 and Jun 4, 2024 — 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.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 4, 2024Break; Break
THE FOLLOWING WAS REPORTED VIA MDR REPORT NUMBER MW5154082: "AT APPROXIMATELY 0855 DURING A LAPAROSCOPIC HYSTERECTOMY DR. INSERTED A 5MM LAPAROSCOPIC TENACULUM THROUGH A 5MM PORT INTO THE PATIENT'S INFLATED ABDOMEN. UPON OPENING THE JAWS OF THE TENACULUM, THE INSTRUMENT SPONTANEOUSLY BROKE LEAVING A SCREW INSIDE THE PATIENT'S ABDOMEN. THE JAWS OF THE TENACULUM WERE THEN STUCK OPEN INSIDE THE ABDOMEN WITHOUT THE ABILITY TO REMOVE SAFELY THROUGH THE PORT, TRAPPING THE INSTRUMENT INSIDE THE BODY. DR. WAS ABLE TO REMOVE THE INSTRUMENT BY SIMULTANEOUSLY REMOVING THE PORT AND INSTRUMENT TOGETHER. THE SCREW WAS RETRIEVED SUCCESSFULLY BY DR. AND PLACED IN THE NEEDLE COUNTER ON THE SURGICAL FIELD BY THE CST. OR MANAGER, WAS INFORMED OF THE INCIDENT. MANAGER RESPONDED TO OR7 TO EVALUATE THE INSTRUMENT. STERILE PROCESSING DEPARTMENT DIRECTOR, WAS ALSO MADE AWARE OF THE INCIDENT. SURGERY CONTINUED BY DOCTORS END OF REPORT. A POSTOPERATIVE X-RAY WAS COMPLETED. THE INSTRUMENT WAS SEQUESTERED AND THE ITEM RECOVERED WAS PLACED IN A SPECIMEN CUP. THIS WAS ALSO REFERRED TO QUALITY. A NOTE WAS PLACED BY THE SURGEON AND THE SURGEON DISCLOSED THIS INFORMATION TO THE PATIENT." IT WAS SUBSEQUENTLY REPORT
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19464427 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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