Olympus A64840ARecalls & reported problems
OLYMPUS Winter & Ibe GmbH · Jaws "HiQ+", 5 x 330 mm, scissors, Mini-Metzenbaum · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04042761027410), received between Dec 10, 2024 and Dec 10, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (2 reports).
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
- Electrical /Electronic Property Problem2
Patient problems
- Unspecified Tissue Injury2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 10, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
ADDITIONAL INFORMATION RECEIVED FROM CUSTOMER REPORTS THE SEROSAL BOWEL INJURY WAS TREATED WITH 3-0 SILK SUTURES OVER THE AREA OF INJURY DURING SURGERY, AND THAT THE PATIENT REQUIRED HOSPITAL STAYS FOR THE SUBSEQUENT HEMODIALYSIS TREATMENTS.
Patient problems: Unspecified Tissue Injury
MAUDE report 20898650 ↗InjuryDec 10, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
ADDITIONAL INFORMATION RECEIVED FROM CUSTOMER REPORTS THE SEROSAL BOWEL INJURY WAS TREATED WITH 3-0 SILK SUTURES OVER THE AREA OF INJURY DURING SURGERY, AND THAT THE PATIENT REQUIRED HOSPITAL STAYS FOR THE SUBSEQUENT HEMODIALYSIS TREATMENTS. THIS REPORT IS RELATED TO THE FOLLOWING LINKED PATIENT IDENTIFIER: (B)(6).
Patient problems: Unspecified Tissue Injury
MAUDE report 20898642 ↗
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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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