Devices

Device Recall AquaPak Sterile Water for Inhalation, USP, 760 mL

Model / Serial
catalog number 037-00, lot 150150, exp. 2009-10
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Colorado, Nebraska, Oregon, Minnesota, California, Pennsylvania, Michigan, Louisiana, Oklahoma and Texas.
Product Description
AquaPak Sterile Water for Inhalation, USP, 760 mL blow-molded plastic bottle for use with a respiratory gas humidifier; 10 bottles per case; manufactured by Hudson Respiratory Care, Inc., Temecula, CA 92589-9020 USA; catalog #037-00
Manufacturer
Teleflex Medical
1 Event
- Recall of Device Recall AquaPak Sterile Water for Inhalation, USP, 760 mL

Manufacturer

Teleflex Medical

Manufacturer Address
Teleflex Medical, 2345 Waukegan Rd Ste 120, Bannockburn IL 60015-1580
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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