Sklar® 96-2504CRecalls & reported problems
Sklar Corporation · IRIS SCISSOR STR 4.5 CS/50 · Class 1
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 50649111170575), received between Feb 7, 2019 and Feb 7, 2019 — 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
- Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 7, 2019Break
RN REPORTED A NEW STERILE PACKAGE OF IRIS SCISSORS WAS OPENED AND SCISSORS IMMEDIATELY BROKE CAUSING THE NURSE TO SUSTAIN A PUNCTURE. THERE WAS NO SERIOUS HARM TO THE NURSE OR THE PATIENT. AN EMPLOYEE INJURY FORM WAS COMPLETED AND THE SCISSORS ARE BEING RETURNED TO THE MANUFACTURER BY THE NURSING UNIT. MANUFACTURER RESPONSE FOR SCISSORS, GENERAL, SURGICAL, SKLAR® (PER SITE REPORTER). THE NURSING UNIT CONTACTED SKLAR CORP DIRECTLY. A COMPLAINT FILE WAS OPENED AND THE DEVICE WILL BE RETURNED FOR FAILURE ANALYSIS. THE STATUS IS CURRENTLY UNKNOWN, BUT WILL BE SHARED WHEN/IF IT BECOMES AVAILABLE.
Patient problems: Injury
MAUDE report 8314397 ↗
Other SCISSORS, GENERAL, SURGICAL devices
- MEDLINE DYNJ04049Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls2 reports
- MEDLINE DYND04000Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls0 reports
- Centurion 66155Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall1 report
- Sklar Instruments 96-2673ASklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2266Sklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2502Sklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion TRI67630Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2492ASklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
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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