Cook recalls Sof-Flex Multi-Length Ureteral Stent Sets with specific product numbers due to risk of stiff wire guide tip entering patient during use.
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 Sof-Flex Multi-Length Ureteral Stent Sets with certain product numbers because the wire guide might be loaded incorrectly. This could cause the stiff tip of the wire guide to enter the patient instead of the flexible tip, potentially causing injury.
The wire guide may be incorrectly loaded into the wire guide holder, causing the stiff tip to be introduced into the patient instead of the flexible tip. This could lead to injury during the procedure.
Patients undergoing ureteral stent procedures who use the recalled Sof-Flex Multi-Length Ureteral Stent Sets with specific product numbers are affected. Medical professionals performing these procedures are most at risk.
Check the product numbers listed: G14773, G15000, G14867, G14951, G17852, 8011038, NS7998389, NS8008388, NS8018651, NS8030247, NS8037667, 7990842, 8599605, 8625597, 8625598, 8172131, 8172132, 8193001.
Identify if your stent set includes any of the listed product numbers: G14773, G15000, G14867, G14951, G17852, 8011038, NS7998389, NS8008388, NS8018651, NS8030247, NS8037667, 7990842, 8599605, 8625597, 8625598, 8172131, 8172132, 8193001.
The recall does not specify if the product is safe to use; it only identifies the risk of incorrect loading leading to potential injury.
The recall does not provide specific action steps for affected users.
Check the product numbers listed: G14773, G15000, G14867, G14951, G17852, 8011038, NS7998389, NS8008388, NS8018651, NS8030247, NS8037667, 7990842, 8599605, 8625597, 8625598, 8172131, 8172132, 8193001.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0976-2020 — Cook Cook Hello, I own a Cook that is covered by recall Z-0976-2020 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.
