Cook recalls Beacon Tip 5.0 Fr Angiographic catheters with specific lot numbers due to potential tip separation. Affected units may require replacement to prevent complications during medical procedures.
Cook Medical identified that catheters supplied in the affected device lots may experience tip separation.
Cook is recalling Beacon Tip 5.0 Fr Angiographic catheters that may experience tip separation. This could lead to complications during medical procedures if the catheter separates during use. Affected units have specific lot numbers listed in the recall.
The catheters may separate at the tip during use, which could cause blockages or complications in the blood vessels. This separation might occur during medical procedures, potentially leading to adverse events.
Healthcare professionals using these catheters in medical procedures are most at risk. Patients receiving these catheters during procedures may be affected if the tip separates.
Check the lot number on the catheter packaging. Affected units include specific lot numbers listed in the recall, such as 15881668, 15903001, and others.
Look for the lot number on the catheter packaging to determine if it's affected.
If the lot number is affected, contact Cook for instructions on replacement or return.
The catheters may experience tip separation during use, which could cause complications in blood vessels during medical procedures.
Check the lot number on the catheter packaging. Affected units have specific lot numbers listed in the recall, such as 15881668, 15903001, and others.
No, but if your lot number is affected, contact Cook for instructions on replacement or return.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-1902-2025 — Cook Cook Hello, I own a Cook that is covered by recall Z-1902-2025 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.
