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
225 of 225 codes
5540UDI10841156100513Lots 643376633647639516645032649315650991656191658151659443660590666438670586672660635207636898643051644573645360645482648481649729650018650873651457653053655645655738657627658250658824659122659217660910661139663039663344665098665099666559668703671743671948672894633211635208635542636901637832644015646106649078650765654190657517657680660717662903
- Model Number
- Amount recalled
- 89,121 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.
Free recall alerts
Get alerted about new Vascular Solutions, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.