Reported Sep 3, 2014 · Terminated
H4052 Endo Tube Holder, Pedi 3.0mm Pediatric Endotracheal Intubation Kit
Smiths Medical ASD, 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: Smiths Medical ASD, Inc. · 10 Bowman Dr · Keene, NH · 03431-5043
Is this the product you have?
- H4052 Endo Tube Holder, Pedi 3.0mm Pediatric Endotracheal Intubation Kit
- Lot codes and dates
- Lot Numbers
65 of 65 codes
2602399258862525807992576366252367925131192492246248185524746472465829245775424433792438616243345124282152412146239406123803522376566236545423615792357822234764223433122343311232958423228272309473229875522987542286596227135922500542244752224475122283642211930220819621919312188460217923121750572154535215205421463012142179213598421286362120121211610021090192090224207718020681232063991206399011889118701185911697
- Lot Numbers
- Amount recalled
- 135,518 (110,246 nationwide)
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
Stop using this product now
The tube fastener on the ET Tube Holder may compress the tracheal tube when used which may cause difficulty when locking the ET Tube Holder in place or difficulty when passing a suction catheter.
Using this product could cause serious injury, illness or death — stop using it now.
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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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