Cook recalls Torcon NB Advantage Catheters due to potential sterility compromise from undersealed packaging. Affected units have specific lot numbers and UDI codes. Consumers should check their product details to determine if recalled.
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 if the catheters are used without proper sterility.
The catheters' packaging pouches may have an undersealed chevron, which could compromise sterility during use. If the packaging is not properly sealed, the catheters might become contaminated, increasing infection risk.
Physicians using these catheters in vascular procedures are most at risk. The recall affects specific lot numbers and UDI codes sold for medical use.
Check for lot number NS9906245 or UDI code (01)00827002089853(17)220801(10)NS9906245 on the packaging. These catheters were sold for use in vascular procedures by trained physicians.
Look for lot number NS9906245 or UDI code (01)00827002089853(17)220801(10)NS9906245 on the packaging.
The recall indicates a potential sterility risk, so affected units should not be used until the remedy is applied.
Check your product details for the lot number or UDI code to determine if you have a recalled unit.
The recall record does not specify a replacement process or remedy.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0456-2020 — Cook Cook Hello, I own a Cook that is covered by recall Z-0456-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.