Reported Feb 18, 2015 · Terminated
AQUAPAK 340 SW, 340, ML W/040, ADAPTOR, JAPA. Product Usage: The Humidifier Adaptor is an accessory which allows…
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 · 2917 Weck Dr · Research Triangle Park, NC · 27709-0186
Is this the product you have?
AQUAPAK 340 SW340ML W/040ADAPTORJAPA
- Product UsageThe Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged with the water bottle is affected by this recall
- Lot codes and dates
- Product Code003-40J
- Lot numbers
64 of 64 codes
149147017147165147337137400137240137492137015147163147151147118147613137130137398137180137244137406137169147212137427137627137152147019147570137329137166147168147164147401137141147160147142147487137490137115147162147170147171147624137619137486137326137437137335137184137409137422137140147332137143147412137105147566137419137241137403137528137616137111147109147
- Amount recalled
- 15,779,607 units
This recall covers 18 products
The agency filed one notice per product. You are reading one of them; the other 17 are below.
5 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
The packages may contain foreign material (black particles).
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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