Abbott Vascular recalls 20/30 Priority Pack Accessory Kit/.096 RHV (REF: 1000186) used in vascular procedures due to potential air embolism risk 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 vascular procedure kit that may leak air during use, which could cause air embolism. This is serious and requires immediate action to prevent health risks.
The inflation device used in vascular procedures can leak air at the hose rotating luer or gauge. This leakage could lead to air embolism, a serious condition where air enters the bloodstream.
Healthcare professionals using this kit during vascular procedures are most at risk. Patients undergoing these procedures may also be affected if the kit is used incorrectly.
Check for the product name '20/30 Priority Pack Accessory Kit/.096 RHV' with reference number 1000186. The kit was sold with specific lot numbers: 60538750, 60538751, 60539113, 60545329.
Immediately stop using the recalled 20/30 Priority Pack Accessory Kit/.096 RHV (REF: 1000186) if it is part of your vascular procedure equipment.
The recalled kit is the 20/30 Priority Pack Accessory Kit/.096 RHV with reference number 1000186.
Leaking air could lead to air embolism, a serious condition where air enters the bloodstream.
Check for the product name '20/30 Priority Pack Accessory Kit/.096 RHV' with reference number 1000186 and lot numbers 60538750, 60538751, 60539113, or 60545329.
We’ve drafted a message you can send Abbott Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-0731-2025 — Abbott Vascular Abbott Vascular Hello, I own a Abbott Vascular that is covered by recall Z-0731-2025 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.
