Reported Jun 26, 2019 · Terminated
Hudson RCI Sheridan LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management
Teleflex Medical
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: Teleflex Medical · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437
Is this the product you have?
- Hudson RCI Sheridan LTS
- Product Code 5-11112 Product UsageTracheal tube/airway management
- Lot codes and dates
- Lot Numbers
73K160036973L160001173A170064673C170023873D170062573E170047573F170038773H170004173H170048373J170029273L170050373M170045373A180067173B180035073D180013873F180017473G180012673G180080673J180030873K180017373L180022573K1800172
- Lot Numbers
- Amount recalled
- 3483 units
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the Endotracheal tube.
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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