Reported Jan 1, 2025 · Ongoing
20/30 Priority Pack Kit/.115 RHV, REF: 1000186-115, used for cardiovascular procedures.
Abbott Vascular Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Abbott Vascular Inc · 26531 Ynez Rd · Temecula, CA · 92591-4630
Is this the product you have?
- 20/30 Priority Pack Kit/.115 RHV
- REF1000186-115, used for cardiovascular procedures
- Lot codes and dates
- UDI-DI08717648015274
- Lots
605649206056493360566431605664326056643360566667
- Amount recalled
- 4,975
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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