Talon 00711175Recalls & reported problems
US Endoscopy · The Talon grasping device is used to retrieve of foreign bodies, tissue specimens, stones or calculi in endoscopic procedures of the gastrointestinal tract. · Class 2
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 00724995182786), received between Nov 13, 2024 and Nov 13, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device 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. 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
- Use of Device 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.
MalfunctionNov 13, 2024Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THEIR TALON GRASPING DEVICES DID NOT PERFORM AS INTENDED DURING A PATIENT PROCEDURE. ANOTHER TALON GRASPING DEVICE WAS UTILIZED TO SUCCESSFULLY COMPLETE THE PROCEDURE RESULTING IN A SHORT DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20678239 ↗
Other DISLODGER, STONE, FLEXIBLE devices
- Stone Cone M0063903200Boston Scientific Corporation · DISLODGER, STONE, FLEXIBLE87 reports
- Stone Cone M0063903100Boston Scientific Corporation · DISLODGER, STONE, FLEXIBLE21 reports
- OLYMPUS NT4F19115Gyrus ACMI, LLC · DISLODGER, STONE, FLEXIBLE6 reports
- OLYMPUS NT4W18115Gyrus ACMI, LLC · DISLODGER, STONE, FLEXIBLE4 reports
- OLYMPUS NT4W22115Gyrus ACMI, LLC · DISLODGER, STONE, FLEXIBLE2 reports
- GYRUS ACMI 5711012Gyrus ACMI, LLC · DISLODGER, STONE, FLEXIBLE2 reports
- GYRUS ACMI 5710009Gyrus ACMI, LLC · DISLODGER, STONE, FLEXIBLE1 report
- OLYMPUS NT4W30115Gyrus ACMI, LLC · DISLODGER, STONE, FLEXIBLE1 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 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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