Angiotech recalls Bone Marrow Biopsy Needles with potential sterile seal defects that could compromise safety during medical procedures.
Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
Angiotech is recalling certain Bone Marrow Biopsy Needles due to a manufacturing issue that may affect the sterile seal. This could lead to contamination or infection risks during medical procedures.
The sterile seal on the blister tray may not form properly, potentially allowing contamination of the needle. This could increase infection risk during medical procedures.
Medical professionals using the recalled needles for bone marrow biopsies are most at risk. Patients receiving these procedures may also be affected.
Check for the model number UCIN-11-10 and lot number LFDB on the product packaging. The product is sold by Angiotech.
Look for model number UCIN-11-10 and lot number LFDB on the packaging.
Argon Medical identified an internal manufacturing issue affecting the sterile seal on some blister trays for the Bone Marrow Biopsy Needle product line.
The official recall notice does not specify a remedy or action steps for affected products.
The recall indicates a potential contamination risk during medical procedures, but no specific injury mechanism is described.
We’ve drafted a message you can send Angiotech to request your refund or repair — edit it as you like.
Subject: Recall Z-0819-2019 — Angiotech Angiotech Hello, I own a Angiotech that is covered by recall Z-0819-2019 from Angiotech. 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.
