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MAGNUM MN1810Recalls & reported problems

Bard Peripheral Vascular, Inc. · MAGNUM® Disposable Core Tissue Biopsy Needle, 18g x 10cm · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741084324), received between Oct 10, 2022 and Oct 10, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Material Twisted/Bent” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Material Twisted/Bent1

Patient problems

  • Pneumothorax1

Recent adverse event reports

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

  • InjuryOct 10, 2022Material Twisted/Bent; Adverse Event Without Identified Device or Use Problem; Material Twisted/Bent; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT DURING AN X-RAY GUIDED LUNG BIOPSY PROCEDURE THROUGH NORMAL DENSITY TISSUE, THE NEEDLE OF THE DEVICE WAS ALLEGEDLY FOUND BENT. NO COAXIAL WAS USED AND THE PROCEDURE WAS COMPLETED USING ANOTHER DEVICE. REPORTEDLY, PATIENT EXPERIENCED PNEUMOTHORAX. CURRENT STATUS OF PATIENT IS UNKNOWN.

    Patient problems: Pneumothorax

    MAUDE report 15568629 ↗

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.