KMEDIC IPN013164Recalls & reported problems
Teleflex Incorporated · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 24026704263008), received between Apr 5, 2023 and Jun 7, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (3 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
- Break3
Patient problems
- Insufficient Information2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 7, 2024Break; Break
IT WAS REPORTED FROM AN ANIMAL HOSPITAL "BREAK AT THE TIP". NO PATIENT INJURY OR CONSEQUENCE REPORTED.
Patient problems: Insufficient Information
MAUDE report 19484217 ↗MalfunctionJun 3, 2024Break; Break
IT WAS REPORTED FROM AN ANIMAL HOSPITAL "ONE PAIR OF THE SCISSORS BROKE WITH A SIMPLE TRIM OF SUTURE ( 3-0 VICRLY), AND THE SECOND WAS A SIMPLE TRIM OF EYELID TISSUE . NOTHING EVER NOTED PRIOR TO SCISSORS BREAKING. ABLE TO FINISH PROCEDURES WITH OTHER SCISSORS. BOTH PATIENTS RECOVERED WITHOUT INCIDENT. " NO PATIENT HARM OR INJURY REPORTED.
Patient problems: Insufficient Information
MAUDE report 19449228 ↗MalfunctionApr 5, 2023Break; Break
IT WAS REPORTED THAT THE TIP BROKE OFF DURING SURGERY. THERE WAS NO PATIENT HARM OR INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16683460 ↗
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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