Bard recalls 10 units of misbranded bone marrow biopsy trays and needles due to incorrect labeling. Affected items may not be safe for medical use without proper identification.
Due to misbranded products shipped to customers.
Bard is recalling 10 units of bone marrow biopsy trays and needles because they were shipped with incorrect labels. This could lead to improper medical use if the items aren't correctly identified.
The products were misbranded, meaning they were labeled incorrectly. This could cause confusion about which items are being used for medical procedures, potentially leading to incorrect procedures.
Medical professionals who use these specific trays and needles for bone marrow biopsies may be affected. Patients receiving these procedures are at risk if the wrong items are used.
Check for the catalog number BEK4511 and the specific model of bone marrow biopsy tray and needles. These items were sold by Bard Peripheral Vascular Inc.
Look for the catalog number BEK4511 on the product to confirm it is part of the recall.
The products were misbranded, so they may not be safe for medical use without proper identification. Do not use until confirmed safe.
Bard is recalling 10 units of the specific bone marrow biopsy trays and needles.
Check the product label for the catalog number BEK4511. If it matches, 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-0153-2022 — Bard Bard Hello, I own a Bard that is covered by recall Z-0153-2022 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.
