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Baxter’s Recall Of Spectrum Infusion Pumps Given Class I Label By FDA

 
• By Shawn M. Schmitt

The US agency said the device maker initiated the recall in December because the pumps might not alarm for repeated occlusion events.

Baxter building in Mississauga, Ontario.
• Source: Shutterstock

The US Food and Drug Administration on 11 March labeled a recall of Baxter Healthcare’s Sigma Spectrum infusion pumps as high-risk class I.

The agency said the company initiated the recall on 29 December because its Spectrum Infusion Pumps with Master Drug Library...

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