FDAnews Device Daily Bulletin
Medical Devices / Postmarket Safety

BD Recalls Infusion Pumps

July 19, 2019
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Beckton Dickinson is recalling its Alaris infusion pumps over potentially weakened bezel plastic.

The affected product, the Alaris Pump Model 8100, has bezel mechanical assemblies made with FR-110 plastic between April 2011 and June 2017 that may have been weakened during the manufacturing process.

“The separation of one or more bezel posts may result in free flow, over infusion, under infusion or interruption of infusion,” the FDA said, advising users to disconnect the device if infusion occurs at an unexpected rate.

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