Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
20/30 Priority Pack Accessory Kit/.096 RHV Recalled by Abbott Vascular Inc Due to Inflation Device used during cardiovascular procedures may leak...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Abbott Vascular Inc directly.
Affected Products
20/30 Priority Pack Accessory Kit/.096 RHV, REF: 1000186, or use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound devices).
Quantity: 3,673
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 39 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MS, MO, MT, NE, NV, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, DC
About Abbott Vascular Inc
Abbott Vascular Inc has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report