Skip to content

Integra® Jarit® 320185Recalls & reported problems

Integra Lifesciences Production Corporation · Integra® Jarit® Debakey Bulldog Clamp, 5", Cardio-Grip ring handle, angled 45°, 40mm jaw · Class 2

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 10381780134367), received between Feb 24, 2022 and Feb 24, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Twisted/Bent” (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

Device problems

  • Material Twisted/Bent1

Patient problems

  • Hemorrhage/Blood Loss/Bleeding1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 24, 2022Material Twisted/Bent; Material Twisted/Bent

    DURING VASCULAR SURGERY FOR DIALYSIS ACCESS, THE DEBAKEY RING HANDLE BULLDOG CLAMP WOULD NOT CLOSE PROPERLY TO STOP BLOOD FLOW AND THE ARTERY KEPT BLEEDING OUT. IT WAS REPORTED THAT NO PATIENT DEATH OCCURRED. REPEATED ATTEMPTS HAVE BEEN MADE TO OBTAIN ADDITIONAL INFORMATION ON PATIENT OUTCOME, BUT NONE HAS BEEN FORTHCOMING.

    Patient problems: Hemorrhage/Blood Loss/Bleeding

    MAUDE report 13590223 ↗

Other CLAMP, VASCULAR devices

All CLAMP, VASCULAR devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.