Skip to content

MARQUEE MQ1213Recalls & reported problems

Bard Peripheral Vascular, Inc. · MARQUEE® Disposable Core Biopsy Instrument, 12g x 13cm · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 1 still open.

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.

Recalls naming this device

  1. Sep 30, 2024Open, Classified

    Disposable biopsy instruments were potentially manufactured missing the backend notch retention feature on the needle that results in inadequate securing of the needle inside the device, which could lead to needle detachment and misplacement, which could lead to tissue damage and bleeding.

    Z-0467-2025 · Root cause: Process change control · FDA record ↗

  2. Jan 14, 2021Terminated

    Due to the Penetration Depth Switch used to select the desired penetration depth of the biopsy needle for soft tissue biopsies, detaches from the device during use.

    Z-1289-2021 · Root cause: Process control · FDA record ↗

Other INSTRUMENT, BIOPSY devices

All INSTRUMENT, BIOPSY devices →

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