Cook recalls Angled Tip Ureteral Catheter Sets with Bentson PTFE Wire Guide due to risk of stiff wire guide tip entering patient during use. Affected models include Global Product Nos G19108, G14587, G15302, G14326, 8018728, 8080823, 8314382, 8409523, 8023194, 7857489.
The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
Cook is recalling Angled Tip Ureteral Catheter Sets with Bentson PTFE Wire Guide because the wire guide might be loaded incorrectly, causing the stiff tip to enter the patient instead of the flexible tip. This could lead to injury during medical procedures.
The wire guide may be loaded incorrectly into the holder, causing the stiff tip to enter the patient instead of the flexible tip. This could lead to injury during medical procedures if the stiff tip is inserted into the wrong part of the body.
Healthcare professionals using the catheter set for medical procedures are most at risk. Patients receiving the catheter during surgery or treatment may be affected if the device is used incorrectly.
Check for the Global Product Numbers: G19108, G14587, G15302, G14326, 8018728, 8080823, 8314382, 8409523, 8023194, or 7857489. The product is sold under the brand Cook.
Identify the Global Product Numbers listed: G19108, G14587, G15302, G14326, 8018728, 8080823, 8314382, 8409523, 8023194, or 7857489.
The recall is for the risk of incorrect loading causing injury. If the wire guide is loaded properly, the product is safe.
The official recall notice does not specify a remedy or action beyond checking product numbers.
Check for the Global Product Numbers: G19108, G14587, G15302, G14326, 8018728, 8080823, 8314382, 8409523, 8023194, or 7857489.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0966-2020 — Cook Cook Hello, I own a Cook that is covered by recall Z-0966-2020 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.
