Comfort Flo Humidification Systems Nebulizer Kits Are Recalled By FDA
Feb 22, 2020 ·
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Description
Vidcast: https://youtu.be/bU_zL3FqcRU Teleflex Medical has been compelled by the FDA to recall four Comfort Flo Humidification System Nebulizer Kits. The kit for the standard unit, the unit with a remote...
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Vidcast: https://youtu.be/bU_zL3FqcRU Teleflex Medical has been compelled by the FDA to recall four Comfort Flo Humidification System Nebulizer Kits. The kit for the standard unit, the unit with a remote temperature port, the corrugated humification system, and the corrugated system with the remote temperature port. This system is used for children and adults to provide heated, humidified air. These units are dangerous since there is a risk of water entering directly into the nose and lungs of the patient. There have been 102 complaints and 8 injuries. Do not use these products. If you as a patient have one of these, you can contact the company at Teleflex Customer Service at 1-866-396-2111. \ https://www.fda.gov/medical-devices/medical-device-recalls/teleflex-medical-recalls-comfort-flo-humidification-systems-due-malfunction-may-cause-water-enter #recall #humidifier
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Information
Author | Howard G. Smith MD |
Website | - |
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