Bard recalls disposable core biopsy kits with specific model numbers due to potential procedure delays or repeat procedures from improper needle fitting.
Coaxial cannula internal diameter and length of biopsy instruments exceed the external diameter and length of the biopsy needle, prohibiting the biopsy needle from properly fitting into the coaxial cannula and accessing the target tissue, which could lead to procedure delay, and insufficient sample acquisition requiring a repeat procedure.
Bard is recalling two types of disposable core biopsy kits because the biopsy needle may not fit properly into the instrument, causing delays or needing a repeat procedure. This affects medical procedures where precise tissue sampling is required.
The biopsy needle's size and shape don't match the coaxial cannula, preventing it from fitting correctly. This can cause the procedure to take longer or require repeating the sample collection, which might delay treatment.
Medical professionals using the Bard Mission Disposable Core Biopsy Instrument Kit for procedures. Patients undergoing biopsies with these kits may face delays or repeat procedures.
Check for model numbers: 2010MSK (20G x 10cm) or 2016MSK (20G x 16cm). The kits were sold with specific expiration dates and lot numbers listed in the product description.
Review the model number and expiration date on the kit packaging to confirm if it matches the recalled items.
The biopsy needle may not fit properly into the coaxial cannula, leading to procedure delays or repeat procedures.
2010MSK (20G x 10cm) and 2016MSK (20G x 16cm).
No action is required if the kit is not the recalled model. Check the model number and expiration date to confirm.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1564-2023 — Bard Bard Hello, I own a Bard that is covered by recall Z-1564-2023 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.
