Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Becton Dickinson (BD) CareFusion 303 Inc. Recalled Alaris System Infusion Pumps Due to Software and System Errors.pic.twitter.com/u2dnMHvUYj

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Becton Dickinson (BD) CareFusion 303 Inc. Recalled Alaris System Infusion Pumps Due to Software and System Errors. pic.twitter.com/u2dnMHvUYj

https://twitter.com/FDADeviceInfo/status/1235936574535327745

Source: Food and Drug Adminstration (FDA): CDRHNew - March 6, 2020 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news

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