Abbott Vascular recalls 20/30 Priority Pack Accessory Kit w/Copilot (REF: 1003327) used in cardiovascular procedures due to potential air embolism from leaks in inflation devices.
Inflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or at the gauge, which could lead to air embolism.
Abbott Vascular is recalling a specific kit used in cardiovascular procedures because it may leak air during use, which could cause air embolism. This is serious and requires immediate attention from medical professionals using the product.
The inflation device in the kit may leak air at the hose rotating luer or gauge during use. This air leakage can travel into the bloodstream, causing air embolism, which is a serious medical emergency.
Healthcare professionals performing cardiovascular procedures who use the recalled kit. Those most at risk are medical staff handling the kit during surgeries or procedures.
Check for the product name '20/30 Priority Pack Accessory Kit w/Copilot' with reference number 1003327. The kit was sold with specific lot numbers listed in the recall notice.
Discontinue use of the recalled kit if it is in your possession.
No, the kit has been recalled due to a risk of air embolism. Do not use it until a replacement is obtained.
Stop using it immediately and contact Abbott Vascular for instructions on returning or replacing it.
Look for the product name '20/30 Priority Pack Accessory Kit w/Copilot' with reference number 1003327 and check the lot numbers listed in the recall notice.
We’ve drafted a message you can send Abbott Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-0732-2025 — Abbott Vascular Abbott Vascular Hello, I own a Abbott Vascular that is covered by recall Z-0732-2025 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.
