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Tricep M0063701230Recalls & reported problems

Boston Scientific Corporation · Hooked-Prong Grasping Forceps · Class 2

Data updated Oct 13, 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 08714729192251), received between Jun 3, 2020 and Jun 3, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 3, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

    IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A TRICEP GRASPING FORCEPS DEVICE WAS TO BE USED IN A URETEROSCOPY PROCEDURE ON (B)(6) 2020. ACCORDING TO THE COMPLAINANT, DURING PREPARATION, A GRASPER WIRE BROKE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH AN UNKNOWN DEVICE. THERE WERE NO PATIENT COMPLICATIONS AS A RESULT OF THIS EVENT. BOSTON SCIENTIFIC HAS BEEN UNABLE TO OBTAIN ADDITIONAL INFORMATION REGARDING THE EVENT TO DATE, DESPITE GOOD FAITH EFFORTS.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10114330 ↗

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Sources and updates

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