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TRUGUIDE C1410ARecalls & reported problems

Bard Peripheral Vascular, Inc. · TRUGUIDE® Disposable Coaxial Biopsy Needle with Depth Stop, 13g x 7.8cm · Class 2

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 00801741084881), received between Jul 23, 2020 and Jul 23, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Remove” (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

  • Difficult to Remove1

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.

  • MalfunctionJul 23, 2020Difficult to Remove; Difficult to Remove

    THIS REPORT SUMMARIZES TWO MALFUNCTIONS. A REVIEW OF THE REPORTED INFORMATION INDICATED THAT MODEL C1410A BIOPSY INSTRUMENT ALLEGEDLY EXPERIENCED DIFFICULTY TO REMOVE. THIS INFORMATION WAS RECEIVED FROM ONE SOURCE. THE MALFUNCTIONS INVOLVED THE SAME PATIENT WITH NO REPORTED PATIENT INJURY. THE FEMALE PATIENT IS (B)(6) YEARS OLD AND WEIGHS (B)(6) KGS.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10315056 ↗

Other Biopsy needle devices

All Biopsy needle devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.