FDA Issues Class I Recall for Q'Apel Medical's 072 Aspiration System Due to Safety Concerns The FDA has classified the voluntary recall of Q'Apel Medical's 072 Aspiration System as Class I, following safety concerns about the device’s distal tip behavior. Details inside.

FDA Issues Class I Recall for Q'Apel Medical's 072 Aspiration System Due to Safety Concerns #United_States #Fremont #Q'Apel_Medical #Aspiration_System #FDA_Recall