Bard recalls Magnum Disposable Core Tissue Biopsy Needles (models MN1410-MN2010) due to possible packaging damage that could compromise sterile barrier. Affected users should check product labels for specific model numbers and lot codes.
Due to possible packaging damage (indentations/cuts) cause by manufacturing process. As a result of the packaging damage, may cause the sterile barrier to be compromised.
Bard is recalling Magnum Disposable Core Tissue Biopsy Needles (models MN1410 to MN2010) because manufacturing may cause packaging indentations or cuts. This could potentially compromise the sterile barrier, risking infection during medical procedures.
The needles come in packaging that may have indentations or cuts from manufacturing. This could allow the sterile barrier to be breached, potentially leading to infection during medical procedures.
Medical professionals using these biopsy needles for tissue sampling are most at risk. Patients undergoing procedures with these needles could face infection if the sterile barrier is compromised.
Check the product label for model numbers: MN1410, MN1420, MN1610, MN1616, MN1820, or MN2010. The packaging may show indentations or cuts that could compromise the sterile barrier.
Look for model numbers on the packaging: MN1410, MN1420, MN1610, MN1616, MN1820, or MN2010.
The recall is due to possible packaging damage (indentations or cuts) from manufacturing that could compromise the sterile barrier.
The affected models are MN1410, MN1420, MN1610, MN1616, MN1820, and MN2010.
If you have the affected models, check the packaging for indentations or cuts. If you find damage, contact Bard for guidance.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-3206-2024 — Bard Bard Hello, I own a Bard that is covered by recall Z-3206-2024 from Bard. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
