Cook recalls Torcon NB Advantage Catheters due to potential sterility compromise from undersealed packaging. Affected units may have contaminated products that could cause infection during medical procedures.
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 their packaging might not seal properly, risking contamination. This could lead to infections during medical procedures if the catheters are used without proper sterility.
The catheters' packaging pouches may have an undersealed chevron, which could compromise sterility. If the packaging isn't sealed properly, the catheters might become contaminated during storage or handling, increasing infection risk during medical procedures.
Physicians using these catheters in vascular procedures are most at risk. The recall affects specific lot numbers and model types sold for coronary and peripheral vascular procedures.
Check for lot number NS9933623 or UDI (01)00827002301634(17)220816(10)NS9933623 on the packaging. These catheters are used in vascular procedures by trained physicians and were sold with specific reference numbers.
Look for lot number NS9933623 or UDI (01)00827002301634(17)220816(10)NS9933623 on the packaging.
The packaging pouches may have an undersealed chevron, which could compromise sterility, potentially leading to contamination during medical procedures.
Check the packaging for lot number NS9933623 or UDI (01)00827002301634(17)220816(10)NS9933623. If you have the affected model, contact Cook for guidance.
The recall indicates a potential sterility risk, so affected units should not be used until the manufacturer provides instructions.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0490-2020 — Cook Cook Hello, I own a Cook that is covered by recall Z-0490-2020 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.
