Abbott Vascular recalls NC TREK Coronary Dilatation Catheters that may have difficulty deflating the balloon, potentially causing complications during procedures.
Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
Abbott Vascular is recalling NC TREK Coronary Dilatation Catheters that may not deflate properly. This could lead to complications during medical procedures if the catheter is used incorrectly.
The catheter's balloon may not deflate correctly, which could cause the catheter to remain inflated during procedures. This might lead to complications like vessel damage or improper treatment.
Healthcare professionals who use these catheters for coronary procedures are most at risk. Patients receiving these catheters during procedures may also be affected.
Check for the product name 'NC TREK Coronary Dilatation Catheter' with reference number 1012455-15. The catheter was sold with lot numbers 90806G1, 91022G1, 90806G2, and 91025G1.
Identify the product by checking the reference number 1012455-15 and lot numbers 90806G1, 91022G1, 90806G2, or 91025G1.
The catheter may have difficulty or inability to deflate the balloon, which could lead to complications during medical procedures.
The official recall notice does not specify a remedy or action steps for consumers.
The recall indicates a potential issue with deflation, so it is recommended to check the product details and follow the manufacturer's guidance.
We’ve drafted a message you can send Abbott Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-1138-2020 — Abbott Vascular Abbott Vascular Hello, I own a Abbott Vascular that is covered by recall Z-1138-2020 from Abbott Vascular. 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.
