Integra® Jarit® 285391Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Woodson Dura Separator And Packer, 7" · 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
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780386438), received between Jan 13, 2023 and Jan 13, 2023 — 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.
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 13, 2023Break; Break
Other INSTRUMENT, SURGICAL, NON-POWERED devices
- SenSight™ B31030Medtronic, Inc. · INSTRUMENT, SURGICAL, NON-POWERED1 recall7 reports
- WECK IPN006432Teleflex Incorporated · INSTRUMENT, SURGICAL, NON-POWERED3 reports
- NA 1120Advanced Neuromodulation Systems, Inc. · INSTRUMENT, SURGICAL, NON-POWERED2 reports
- 3.3mm Mini-Bolt VUE 21133Monteris Medical Inc · INSTRUMENT, SURGICAL, NON-POWERED2 reports
- NA 365538Medtronic, Inc. · INSTRUMENT, SURGICAL, NON-POWERED2 reports
- Integra® Jarit® 285120Integra Lifesciences Production Corporation · INSTRUMENT, SURGICAL, NON-POWERED1 report
- OASYS 48561039Stryker Corporation · INSTRUMENT, SURGICAL, NON-POWERED1 report
- AESCULAP FV002RAesculap AG · INSTRUMENT, SURGICAL, NON-POWERED1 report
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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