Cook recalls Torcon NB Advantage Catheters due to potential sterility compromise from undersealed packaging pouches. Affected lot numbers include 9693491, 9696896, and others. Consumers should check their product details and contact Cook for guidance.
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 in medical procedures. Affected units have specific lot numbers and unique identifiers.
The catheters' packaging pouches may have an undersealed chevron, which could compromise sterility. If the pouch isn't sealed properly, the catheters might become contaminated during use, increasing infection risk.
Physicians using Torcon NB Advantage Catheters for vascular procedures are likely affected. Patients undergoing procedures with these catheters could be at risk if the product is contaminated.
Check for lot numbers 9693491, 9696896, 9700377, 9700378, 9700379, 9710398, 9716496, or NS9712994. Also look for unique identifiers starting with (01)00827002072688.
Identify your lot number and unique identifier to confirm if your Torcon NB Advantage Catheters are affected.
Reach out to Cook Inc. for further guidance on handling affected products.
The recall indicates a potential sterility risk, so affected units should not be used until confirmed safe by Cook.
Affected lot numbers include 9693491, 9696896, 9700377, 9700378, 9700379, 9710398, 9716496, and NS9712994.
Check the lot number and unique identifier on the packaging, which are listed in the recall notice.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0448-2020 — Cook Cook Hello, I own a Cook that is covered by recall Z-0448-2020 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.
