Medicamentos del Reino Unido y Productos Sanitarios (MHRA) ha emitido una alerta de dispositivo para el grupo Teleflex Medical SMO cánula de traqueotomía. Diseñado para ser insertadas quirúrgicamente en la tráquea del paciente para mantener abiertas las vías respiratorias, el aparato está siendo retirado del mercado debido a un error de fabricación. El tubo del conjunto es demasiado recto, lo que eleva el riesgo de lesiones en la pared traqueal de un paciente durante la inserción o en el tiempo después de la inserción.
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MHRA Issues Device Alert for Teleflex Tracheostomy Set
The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has issued a device alert for Teleflex Medical’s GOS tracheostomy canula set. Designed to be surgically inserted into a patient’s trachea to maintain an open airway, the set is being recalled due to a manufacturing error. The set’s tube is too straight, which raises the risk of injury to a patient’s tracheal wall during insertion or over time following insertion.
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MHRA Issues Device Alert for Teleflex Tracheostomy Set
The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has issued a device alert for Teleflex Medical’s GOS tracheostomy canula set. Designed to be surgically inserted into a patient’s trachea to maintain an open airway, the set is being recalled due to a manufacturing error. The set’s tube is too straight, which raises the risk of injury to a patient’s tracheal wall during insertion or over time following insertion.
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