Cook recalls Torcon NB Advantage Catheters due to potential sterility compromise from undersealed packaging pouches. Affected units sold in specific lots and UDI numbers. Consumers should check product details and contact Cook for remedy.
The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.
Cook is recalling Torcon NB Advantage Catheters because the packaging pouches might not seal properly, risking contamination. This could lead to infections if the catheters are used. The recall affects specific lots and units sold to medical professionals.
The catheters' packaging pouches may have an undersealed chevron, which could allow contamination. If the packaging is compromised, the catheters might not be sterile when used in procedures, increasing infection risk.
Medical professionals who use Torcon NB Advantage Catheters for vascular procedures are most at risk. Patients receiving these catheters during procedures may also be affected if the catheters are contaminated.
Check the lot number (9906464) and UDI number (01)008270:002115439(17)220801(10)9906464 on the packaging. These units were sold to medical professionals for vascular procedures.
Look for the lot number 9906464 and UDI number (01)00827002115439(17)220801(10)9906464 on the packaging.
The packaging pouches may have an undersealed chevron, which could compromise sterility and lead to contamination.
Check the lot number and UDI number on the packaging. If you have the affected units, contact Cook for further instructions.
The recall addresses potential contamination risk, not direct injury. The hazard is low risk as it relates to sterility, not immediate harm.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0480-2020 — Cook Cook Hello, I own a Cook that is covered by recall Z-0480-2020 from Cook. 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.
