Cook recalls Torcon NB Advantage Catheters due to potential sterility compromise from undersealed packaging. Affected units may have contaminated products. 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 may not seal properly, risking contamination. This could lead to infections if used in medical procedures. The recall affects specific lot numbers and requires action to ensure product safety.
The catheters' packaging pouches may have an undersealed chevron, which could compromise sterility during use. This risk exists if the product is used in medical procedures without proper sterility.
Physicians using Torcon NB Advantage Catheters for vascular procedures are most at risk. The recall applies to specific lot numbers sold between 2019 and 2020.
Check for lot number 9903997 or UDI (01)00827002061088(17)220801(10)9903997 on the packaging. The product was sold between 2019 and 2020 for vascular procedures by trained physicians.
Look for lot number 9903997 or UDI (01)00827002061088(17)220801(10)9903997 on the packaging.
The packaging pouches may have an undersealed chevron, which could compromise sterility during medical procedures.
Check the lot number or UDI on the packaging. If it matches the recalled numbers, contact Cook for instructions.
The recall addresses potential sterility compromise, which could lead to infections. However, the remedy does not specify immediate action for serious injury.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0440-2020 — Cook Cook Hello, I own a Cook that is covered by recall Z-0440-2020 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.
