Defibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and Lifeline Auto (DDU-l XX Series)-Indicated for use on victims of sudden cardiac arrest (SCA.)
Publicado el 4 de diciembre de 2024 · Inicio del retiro: 14 de octubre de 2024
Estado reportado al momento de publicación: Ongoing — openFDA actualiza semanalmente y este campo no refleja el estado más reciente. Confirma siempre con la fuente oficial.
Qué peligro representa
Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could potentially lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life.there is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient
Qué hacer
Voluntary: Firm initiated · E-Mail
Detalles del retiro
- Fabricante
- Defibtech, LLC
- Distribuidor
- Ireland
- Lote
- UDI-DI: 00815098020430, DDP-200P pediatric defibrillation pads, single pair; 10815098020437, DDP-200P pediatric defibrillation pads, single pair configuration; 40815098020438, DDP-200P pediatric defibrillation pads, 20 pairs
- Clasificación de riesgo
- Class II
- Área (FDA)
- device
- País
- United States
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