FDAFDA · Alimentos y medicamentos·N.º oficial Z-0487-2015
Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integral hook strip (i.e., Velcro) to allow for the use of a loop material to help secure a nasal interface. The Cannulaide is applied under and over the nose of infants to provide a protective barrier to the philtrum, columella, septum, nares, and tip of nose. It is available in multiple sizes that vary the external geometry and nare hole size and spacing to allow for use on infants ranging from less than 700 grams to greater than 3000 grams. It is a non sterile, single patient use, disposable device.
Publicado el 10 de diciembre de 2014 · Inicio del retiro: 18 de enero de 2007
Estado reportado al momento de publicación: Terminated — openFDA actualiza semanalmente y este campo no refleja el estado más reciente. Confirma siempre con la fuente oficial.
Qué peligro representa
Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.
Qué hacer
Voluntary: Firm initiated · E-Mail
Detalles del retiro
- Fabricante
- Beevers Manufacturing & Supply, Inc.
- Distribuidor
- Worldwide Distribution: US (nationwide) and country of: ME-Musaffah.
- Lote
- Lot 20060928. Product expired in 2009.
- Clasificación de riesgo
- Class II
- Área (FDA)
- device
- País
- United States
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