Integra® Jarit® 106220Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Rochester-Ochsner Forceps, 7-3/4", Straight, 1x2 Teeth, Satin Finish · Class 1
All models of Integra Jarit (57)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10381780023845), received between Sep 22, 2023 and Jul 14, 2025 — classified as 2 malfunctions.
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
- Mechanics Altered1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 14, 2025Break; Break
A FACILITY REPORTED THAT DURING A TOTAL KNEE REPLACEMENT, THE OCHSNER FCPS 8 STR SATIN (106220) BROKE AT THE JAW. THE BROKEN JAW WAS RECOVERED, AND ANOTHER INSTRUMENT WAS USED TO COMPLETE THE SURGERY. NO INJURIES, DEATHS, OR SURGICAL DELAYS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22501491 ↗MalfunctionSep 22, 2023Mechanics Altered; Mechanics Altered
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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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