Integra® Jarit® 135181Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Babcock Forceps, 6", Tissue, 8mm Wide · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780433460), received between May 29, 2026 and May 29, 2026 — classified as 1 injury.
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
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 29, 2026Break
A FACILITY REPORTED THAT THE BABCOCK TISS FCPS 6-1/4 (135181) WAS BEING USED IN A PROCEDURE WHEN IT BROKE. IT WAS NOT KNOWN AT THE TIME OF SURGERY THAT THE INSTRUMENT HAD BROKEN. THE BREAK WAS DISCOVERED DURING INSTRUMENT CLEANING. ONCE IDENTIFIED, THE PATIENT WAS BROUGHT BACK TO THE OPERATING ROOM FOR A SECOND SURGERY TO RETRIEVE THE RETAINED PIECE. THE BROKEN PART WAS SUCCESSFULLY RECOVERED. NO DEATH OR INJURY WAS REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 25333944 ↗
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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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