Reported Oct 28, 2020 · Terminated
Langston Dual Lumen Catheter.
Vascular Solutions, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.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: Vascular Solutions, Inc. · 6420 Sycamore Ln N · Maple Grove, MN · 55369-6013
Is this the product you have?
- Langston Dual Lumen Catheter.
- Lot codes and dates
- Model Number
5550UDI 10841156100537 total 2990
- Lots
637973640204659555660597633668663767669593659856644096676528672481632704656792658273666755635885
- Model Number
- Amount recalled
- 2990 units
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
Stop using this product now
The inner lumen of the Langston catheter may separate from the hub during pressure injection.
Using this product could cause serious injury, illness or death — stop using it now.
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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