Comfort Flo Humidification Systems Nebulizer Kits Are Recalled By FDA

22 de feb. de 2020 · 54s
Comfort Flo Humidification Systems Nebulizer Kits Are Recalled By FDA
Descripción

  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...

mostra más
  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  
mostra menos
Información
Autor Howard G. Smith MD
Página web -
Etiquetas

Parece que no tienes ningún episodio activo

Echa un ojo al catálogo de Spreaker para descubrir nuevos contenidos.

Actual

Portada del podcast

Parece que no tienes ningún episodio en cola

Echa un ojo al catálogo de Spreaker para descubrir nuevos contenidos.

Siguiente

Portada del episodio Portada del episodio

Cuánto silencio hay aquí...

¡Es hora de descubrir nuevos episodios!

Descubre
Tu librería
Busca