dimecres, 8 d’octubre del 2014

Teleflex issues Class I recall of pediatric anesthesia devices




Teleflex issues a Class I recall of its pediatric anesthesia devices over concerns that certain components could break during use, resulting in serious injury or even death.





Teleflex issues Class I recall of pediatric anesthesia devices

Food & Drug Administration (FDA), Teleflex

News Well, Anesthesia, Pediatrics, Recalls

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