Cook recalls Torcon NB Advantage Catheters due to potential sterility compromise from undersealed packaging. Affected units have specific lot numbers and were sold for vascular procedures. Consumers should contact Cook for details.
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 may not seal properly, risking contamination. This could lead to infections or other complications during medical procedures. The recall affects specific lot numbers used in vascular treatments.
The catheters' packaging pouches may have an undersealed chevron, which could compromise sterility. If the packaging isn't properly sealed, the catheters might become contaminated during use, increasing infection risk.
Physicians using Torcon NB Advantage Catheters for vascular procedures are most at risk. The recall applies to specific lot numbers sold for coronary and peripheral vascular treatments.
Check for lot number NS9904740 or UDI (01)00827002107960(17)220:220801(10)NS9904740 on the packaging. These catheters were used in vascular procedures by physicians trained in angiographic techniques.
Look for lot number NS9904740 or UDI (01)00827002107960(17)220801(10)NS9904740 on the packaging.
The packaging pouches may have an undersealed chevron, which could compromise sterility.
Check for the specific lot number or UDI on the packaging. Contact Cook for further instructions.
The recall indicates a potential sterility risk, so it's recommended to stop using if you have the affected lot numbers.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0474-2020 — Cook Cook Hello, I own a Cook that is covered by recall Z-0474-2020 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.