Integra® Jarit® 110175Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Knife Handle No. 3, 4-7/8", Holds Blades 10, 11, 12, 15, Matte Finish · 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 10381780433101), received between Oct 23, 2023 and Oct 23, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Product Quality Problem” (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
- Product Quality Problem1
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.
MalfunctionOct 23, 2023Product Quality Problem; Product Quality Problem
Other HANDLE, SCALPEL devices
- HU-FRIEDY K360Hu-Friedy Mfg. CO., LLC · HANDLE, SCALPEL1 recall1 report
- Centurion 66825Centurion Medical Products Corporation · HANDLE, SCALPEL1 recall0 reports
- Centurion I68290Centurion Medical Products Corporation · HANDLE, SCALPEL1 recall0 reports
- NA 03.010.491Synthes GmbH · HANDLE, SCALPEL23 reports
- NA 03.140.027Synthes GmbH · HANDLE, SCALPEL13 reports
- DeRoyal D4511ADeroyal Industries, Inc. · HANDLE, SCALPEL7 reports
- DeRoyal D4522NSDeroyal Industries, Inc. · HANDLE, SCALPEL1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.