Reported Apr 20, 2022 · Ongoing
20/30 Priority Pack w/COPILOT - REF 1003327 WPL2122272-01 (2019-03-01)
Abbott Vascular
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 · 26531 Ynez Rd · Temecula, CA · 92591-4630
Is this the product you have?
- 20/30 Priority Pack w/COPILOT - REF 1003327 WPL2122272-01 (2019-03-01)
- Lot codes and dates
- Part Numbers1003327
- Device Identifier-GTIN08717648013973
- Lot Numbers
131 of 131 codes
603085716031591960325098603085726031640760325099603085736031700460325100603085746031727960325101603085756031728060325103603096716031753360326298603096726031754060326299603096736031754160326300603096746031794760326301603096756031794860326425603096766031866860326859603096776031866960326860603096816031867060326861603096826031981960326862603096836032006760326863603096846032006860328011603096856032006960328023603096866032007060328355603096876032007260328356603113416032007360329330
- Amount recalled
- 131 lots
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Due to an increase in complaint trend for leaks and intermittent/loose connections.
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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