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Q3 Recalls Snapshot: It’s Good News For Industry And Patients As Recall Events, Recalled Units Fall

Executive Summary

Medical device manufacturers initiated fewer recalls in the third quarter of 2020. Check out our Q3 recalls infographic.

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Q2 Recalls Snapshot: Recall Events Rise 31% While Recalled Units Slide

Medical device recalls initiated in the second quarter of 2020 increased 31% from the previous quarter, marking the largest number of corrections and removals in a quarter in two years. Check out our Q2 recalls infographic.

Class I Recall Of Alaris Device Is Pump’s Second In 3 Days

Third-party servicer Tenacore LLC recalled the Model 8100 infusion pumps because patients are at risk of receiving incorrect fluid dosage. The recall was designated as class I by the US FDA on 19 April; it’s the pump’s second class I recall in the span of three days.

US FDA: Recall Of BD Alaris Infusion Pump Is High-Risk Class I

Becton Dickinson’s CareFusion 303 Inc. subsidiary recalled 145,492 of the pumps because there’s a risk that the device’s keypad will lift up and away from the device body if it comes into contact with fluids.





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