Abbott Vascular recalls 20/30 Priority Pack Kit/.115 RHV 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 20/30 Priority Pack Kit/.115 RHV kits used in cardiovascular procedures because they may leak air in the inflation device, leading to air embolism. This hazard affects medical professionals using the kits during procedures.
The inflation device used during procedures may leak air at the hose rotating luer or gauge. This leak can cause air embolism, which is a serious condition where air enters the bloodstream.
Medical professionals who use these kits during cardiovascular procedures are most at risk. Patients undergoing procedures with these kits could be affected if the leak occurs.
Check for the product name '20/30 Priority Pack Kit/.115 RHV' with reference number 1000186-115. The kit was sold with specific lot numbers: 60564920, 60564933, 60566431, 60566432, 60566433, 60566667.
Verify the product name and reference number to confirm if your kit is recalled.
The recall number is not provided in the official notice.
Check for the product name '20/30 Priority Pack Kit/.115 RHV' with reference number 1000186-115 and lot numbers 60564920, 60564933, 60566431, 60566432, 60566433, or 60566667.
The official notice does not specify a remedy, so contact Abbott Vascular directly for 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-0733-2025 — Abbott Vascular Abbott Vascular Hello, I own a Abbott Vascular that is covered by recall Z-0733-2025 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.
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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.
