Integra® Jarit® 121260Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Berry Sternal Needle Holder And Wire Twister, 7-1/4", Carb-Bite, Heavy, 5mm Wide · Class 1
Data updated Oct 13, 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 10381780377627), received between Sep 8, 2021 and Sep 8, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Component Missing” (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.
Most reported problems
Device problems
- Component Missing1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 8, 2021Component Missing
BULLDOG NEEDLEDRIVER: DURING THIS PROCESS THE TIP WAS DISCOVERED TO BE MISSING A PIECE.
Patient problems: Insufficient Information
MAUDE report 12438306 ↗
Other TWISTER, WIRE devices
- NA 03.108.040Synthes GmbH · TWISTER, WIRE1 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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