Class I Medical Device Recall: Medfusion 3500 and 4000 Syringe Pumps

Medfusion 3500 and 4000 Syringe Pumps: Class I Medical Device Recall by US-FDA

On 24-Aug-2020, US-FDA has released a recall alert for class I medical Device- Medfusion 3500 and 4000 Syringe Pumps due to risk of medication delivery error. Device Use: This is used in the delivery of following products into the patient’s body in a controlled manner. Blood Blood products Prescribed medications Other fluids Syringe pumps which

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