FDAFDA · Food and drugs·Recall number Z-1101-2015
AQUAPAK 340 SW, 340, ML W/040, ADAPTOR, JAPA. Product Usage: The 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.
Published February 18, 2015 · Recall initiated: January 14, 2015
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The packages may contain foreign material (black particles).
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Teleflex Medical
- Distributor
- Worldwide Distribution - U.S. Nationwide and the countries of: Australia, Bahrain, Belgium, Bermuda, Brazil, Canada, China, Ecuador, Germany, Great Britain, Hong Kong, Indonesia, Japan, Jordan, Malaysia, Mexico, New Zealand, Philippines, Singapore, South Korea, Saudi Arabia, Taiwan, Thailand, Uruguay and Zambia.
- Lot
- Product Code: 003-40J, Lot numbers: 149147, 017147, 165147, 337137, 400137, 240137, 492137, 015147, 163147, 151147, 118147, 613137, 130137, 398137, 180137, 244137, 406137, 169147, 212137, 427137, 627137, 152147, 019147, 570137, 329137, 166147, 168147, 164147, 401137, 141147, 160147, 142147, 487137, 490137, 115147, 162147, 170147, 171147, 624137, 619137, 486137, 326137, 437137, 335137, 184137, 409137, 422137, 140147, 332137, 143147, 412137, 105147, 566137, 419137, 241137, 403137, 528137, 616137, 111147, 109147, 417137, 181137, 185137, 161147 & 146147.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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