Integra® Jarit® 300150Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Tuffier Rib Spreader, 7" Spread, Roughened Blades · Class 1
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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780456377), received between Mar 24, 2025 and Mar 24, 2025 — 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. 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.
InjuryMar 24, 2025Break; Break
IT WAS REPORTED THAT THE RETRACTOR/TUFFIER RIB SPREADER SCORED) BROKE DURING OPEN DECORTICATION OF RIGHT LUNG. "THE KNOB THAT ALLOWS FOR THE OPENING OF THE RETRACTOR BROKE OFF. THE RETRACTOR WAS IMMEDIATELY REMOVED. ALL THE PIECES WERE RETRIEVED. THE SURGEON HAD TO CUT A PIECE OF RIB OFF IN ORDER TO SEQUESTER ALL THE PIECES. ONCE THE PIECES WERE RETRIEVED, THE DEVICE WAS PLACED OFF THE STERILE FIELD AND BAGGED." IT WAS REPORTED THAT THERE WAS AN UNSPECIFIED DELAY IN PROCEDURE DUE TO THE PRODUCT PROBLEM. A DIFFERENT RETRACTOR WAS USED TO COMPLETE THE CASE. AN X-RAY WAS REPORTEDLY PERFORMED IN THE INTENSIVE CARE UNIT (ICU), AS THE PIECE BROKE OFF CLEANLY."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21679235 ↗
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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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