Reported Mar 26, 2025 · Ongoing

CAPNOCHECK BCI Airway Adapter; Model Number BSR; Product Code WW8214

Smiths Medical ASD, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

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. · 6000 Nathan Ln N · Minneapolis, MN · 55442-1690

Is this the product you have?

  • CAPNOCHECK BCI Airway Adapter; Model Number BSR; Product Code WW8214
Lot codes and dates
  • UDI-DI 30610586038444 Lots

    275 of 275 codes

    • WW8214
    • 022980-1-22
    • 022404-1-17
    • 021860-1-10
    • 021110-1-7
    • 020609-1-2
    • 016288-1-1
    • 022980-1-24
    • 022404-1-18
    • 021860-1-14
    • 021110-1-8
    • 020609-1-3
    • 017774-1-1
    • 022980-1-23
    • 022404-1-19
    • 021860-1-13
    • 021110-1-9
    • 020609-1-4
    • 018139-1-1
    • 022980-1-26
    • 022404-1-20
    • 021860-1-15
    • 021110-1-10
    • 020609-1-5
    • 018184-1-1
    • 022980-1-27
    • 022404-1-21
    • 021860-1-17
    • 021110-1-11
    • 020609-1-6
    • 018252-1-1
    • 022980-1-28
    • 022404-1-22
    • 021860-1-16
    • 021110-1-12
    • 020609-1-7
    • 018458-1-1
    • 022980-1-25
    • 022404-1-23
    • 021860-1-18
    • 021110-1-13
    • 020609-1-8
    • 018457-1-1
    • 022980-1-32
    • 022404-1-24
    • 021860-1-20
    • 021110-1-14
    • 020609-1-9
    • 018614-1-1
    • 022980-1-30
    • 022404-1-25
    • 021860-1-21
    • 021110-1-16
    • 020609-1-10
    • 018641-1-1
    • 022980-1-29
    • 022404-1-26
    • 021860-1-19
    • 021110-1-15
    • 020609-1-11
    /
Amount recalled
175,994 US; 45,223 OUS

This recall covers 14 products

The agency filed one notice per product. You are reading one of them; the other 13 are below.

1 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Airway adapter does not meet specification and may break off when attaching a valve or tube. Device failure may result in inaccurate readings, a break in airway circuit, and loss of ventilation. A break in the airway circuit could result in inability to ventilate, hypoxia, cardiopulmonary collapse, or death.

This product could cause temporary or reversible health problems — stop using it.

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

Data as of Sep 19, 7:38 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.