Integra® Jarit® 600490Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Puncture Needle, 13", with Irrigation, 5mm · Class 2
All models of Integra Jarit (57)
Data updated Oct 16, 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 10381780152255), received between Jan 28, 2025 and Jan 28, 2025 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.
MalfunctionJan 28, 2025Break; Break
A FACILITY REPORTED THAT DURING A LAPAROSCOPIC PROCEDURE, THE TIP OF THE LAPAROSCOPIC ASPIRATION NEEDLE/PUNCTURE NEEDLE W/IRRIG 32CM (600490) BROKE OFF. IT WAS SUBSEQUENTLY REPORTED THAT "THE NEEDLE BROKE OFF WHILE INSIDE THE PATIENT, THEN NEEDED TO BE RETRIEVED AND THEN REMOVED LAPAROSCOPICALLY BY THE SURGEON." ALL BROKEN PARTS WERE RECOVERED. IT WAS REPORTED THAT THERE WAS NO DELAY IN THE PROCEDURE. NO PATIENT INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21258012 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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