Abbott Vascular Inc 2025-01-01 Health serious FDA
Health · FDA · Recall #FDA-Z-0732-2025
20/30 Priority Pack Accessory Kit w/Copilot, REF: 1003327, used for cardiovascular… Recall
Issued January 1, 2025 · Abbott Vascular Inc
In January 2025, Abbott Vascular Inc recalled the 20/30 Priority Pack Accessory Kit w/Copilot, REF: 1003327, used for cardiovascular…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using 20/30 Priority Pack Accessory Kit w/Copilot, REF: 1003327, used for cardiovascular… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Abbott Vascular Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Abbott Vascular Inc
- Category
- Health
- Recall date
- January 1, 2025
- Units affected
- Not reported
- Sold at
- US: IA, MD, DC, IN, CA, NV, TX, CT, GA, MS, NY, OH, FL, NC, MI, KY, PA, VA, IL, OK, TN, UT, WA, WI, MT, OR, LA, HI, NE, AR, MO, MA, KS, ID,
- Recall number
- FDA-Z-0732-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Abbott Vascular Inc has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.