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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 30 Results
510(K) Number: K833974
 
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Product Description
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FDA Recall
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AQUAPAK 340 SW, 340ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory... 2 02/12/2015 Teleflex Medical
AQUAPAK 640 SW, 650ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory... 2 02/12/2015 Teleflex Medical
AQUAPAK 640 SW, 650ML W/040 ADAPTOR, FREN. Product Usage: The Humidifier Adaptor is an accessory... 2 02/12/2015 Teleflex Medical
AQUAPAK 640 SW, 650ML W/040 ADAPTOR, FREN. Product Usage: The Humidifier Adaptor is an accessory... 2 02/12/2015 Teleflex Medical
AQUAPAK SW/EAU STERILE, 650 ML W/ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory ... 2 02/12/2015 Teleflex Medical
AQUAPAK 640 SW, 650ML W/040 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which... 2 02/12/2015 Teleflex Medical
AQUA 540 SW, 540 W/040 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allo... 2 02/12/2015 Teleflex Medical
AQUAPAK 340 SW, 340, ML W/040, ADAPTOR, JAPA. Product Usage: The Humidifier Adaptor is an access... 2 02/12/2015 Teleflex Medical
AQUAPAK 340 SW, 340 ML W/040 ADAPTOR, FREN. Product Usage: The Humidifier Adaptor is an accessor... 2 02/12/2015 Teleflex Medical
AQUAPAK SW/EAU STERILE, 340 ML W/ADAPTOR Product Usage: The Humidifier Adaptor is an accessory w... 2 02/12/2015 Teleflex Medical
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