Is it my imagination or has there been an unusual amount of infusion pump recalls lately?
The Baxter Colleague, the Alaris SE, The Alaris System (Medley) again…!
The equipment downtime and the loss of revenue is paled by the risk to the patient these devices cause. What does all this mean to me? It means that there isn’t enough testing being done before releasing the device to market. I understand that from a manufacturer’s point of view, the only thing that matters is the bottom line. Made by the lowest bidder, indeed!
Whats your take?
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