Reported Jul 16, 2014 · Terminated

Aquapak 340 SW, 340, mL w/040 Adaptor, International, Teleflex Medical, respiratory gas humidifier adaptor .

Teleflex Medical

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: Teleflex Medical · 4024 Stirrup Creek Dr · Durham, NC · 27703-9000

Is this the product you have?

  • Aquapak 340 SW, 340, mL w/040 Adaptor, International, Teleflex Medical, respiratory gas humidifier adaptor .
Lot codes and dates
  • Product Code400340
  • Lot numbers

    97 of 97 codes

    • 082127
    • 085127
    • 088127
    • 092127
    • 094127
    • 097127
    • 100127
    • 102127
    • 104127
    • 106127
    • 108127
    • 137127
    • 141127
    • 145127
    • 148127
    • 154127
    • 156127
    • 159127
    • 161127
    • 163127
    • 194127
    • 198127
    • 200127
    • 204127
    • 207127
    • 209127
    • 223127
    • 224127
    • 226127
    • 228127
    • 230127
    • 232127
    • 239127
    • 241127
    • 243127
    • 245127
    • 246127
    • 248127
    • 250127
    • 252127
    • 256127
    • 259127
    • 263127
    • 266127
    • 269127
    • 289127
    • 290127
    • 292127
    • 307127
    • 309127
    • 312127
    • 314127
    • 316127
    • 318127
    • 320127
    • 322127
    • 338127
    • 340127
    • 345127
    • 350127
Amount recalled
7,758,650 ea. (total for all types listed)

This recall covers 15 products

The agency filed one notice per product. You are reading one of them; the other 14 are below.

2 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

The seals of the respiratory gas humidifier adaptor packaging may be creased which may potentially affect packaging integrity.

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

Notice updated Jul 2, 2015 · Data as of Sep 19, 5:59 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.