Integra® Jarit® 120135Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Mayo-Hegar Needle Holder, 6-1/4", Grooved Jaws · Class 1
- 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 10381780377009), received between Jun 17, 2024 and Jun 17, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Premature Separation” (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
- Premature Separation1
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.
MalfunctionJun 17, 2024Premature Separation; Premature Separation
Other HOLDER, NEEDLE, GASTROENTEROLOGIC devices
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- Capio RP M0068321010Boston Scientific Corporation · HOLDER, NEEDLE, GASTROENTEROLOGIC1 recall0 reports
- Integra® Jarit® 121135Integra Lifesciences Production Corporation · HOLDER, NEEDLE, GASTROENTEROLOGIC4 reports
- NA 26173HAKarl Storz GmbH & Co. KG · HOLDER, NEEDLE, GASTROENTEROLOGIC3 reports
- Integra® Jarit® 121210Integra Lifesciences Production Corporation · HOLDER, NEEDLE, GASTROENTEROLOGIC2 reports
- V. Mueller RH2551Steris Corporation · HOLDER, NEEDLE, GASTROENTEROLOGIC1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.