Reported Sep 3, 2014 · Terminated

H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy, LDS 15mm Conn 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?

  • H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy, LDS 15mm Conn Pediatric Endotracheal Intubation Kit
Lot codes and dates
  • Lot Numbers
    • 2474641
    • 2470638
    • 2453454
    • 2448650
    • 2438611
    • 2433436
    • 2428205
    • 2412133
    • 2400804
    • 2347041
    • 2343292
    • 2326893
    • 2298737
    • 2271338
    • 2260550
    • 2211923
    • 2188448
    • 2175049
    • 2135974
    • 2099500
    • 2068120
    • 2042404
    • 11872
    • 11861
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.

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 26, 2021 · Data as of Sep 19, 6:54 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.