Cook recalls Torcon NB Advantage Catheters due to potential packaging pouch undersealing, risking product sterility. Affected units include specific lot numbers and UDIs. 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 their packaging pouches might not seal properly, which could compromise sterility. This is a serious risk for medical procedures since unsterile catheters could cause infections or other complications.
The catheters' packaging pouches may have an undersealed chevron, which could allow contamination. If the catheters are not sterile when used, they might cause infections or other complications during medical procedures.
Physicians using these catheters in vascular procedures are most at risk. The recall affects specific lot numbers and UDIs sold for coronary and peripheral vascular treatments.
Check for lot numbers NS9906320 or NS9906321 and UDIs starting with (01)00827002107335. These catheters were sold for use in coronary and peripheral vascular procedures by physicians.
Immediately stop using the recalled Torcon NB Advantage Catheters if you have them.
The packaging pouches might not seal properly, which could compromise sterility and lead to infections or complications during medical procedures.
Stop using them immediately and contact Cook for instructions on how to return or dispose of the product.
Lot numbers NS9906320 and NS9906321 are affected, as well as specific UDIs starting with (01)00827002107335.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0467-2020 — Cook Cook Hello, I own a Cook that is covered by recall Z-0467-2020 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.
