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BD Alaris Recalls Flash Insight Report 2020
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BD Alaris Recalls Flash Insight Report 2020

October 2020

Current Time Inside Cache Tag Helper: 9/24/2020 9:26:54 AM and Model.reportId = 1801

Categorized by the FDA as a Class I recall and initiated by BD on February 4, 2020, the most recent recall of BD’s Alaris infusion pumps involves 774,000 devices and was triggered by “multiple system errors, software errors, and use-related errors.” Based on feedback from 53 individuals at 50 Alaris customer organizations, this report examines what impact the recall has had on BD customers’ satisfaction and future plans and whether BD has been successful in addressing patient-safety concerns and minimizing disruption.

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Current Time Inside Cache Tag Helper: 9/24/2020 9:26:54 AM and Model.reportId = 1801

This material is copyrighted. Any organization gaining unauthorized access to this report will be liable to compensate KLAS for the full retail price. Please see the KLAS DATA USE POLICY for information regarding use of this report. © 2020 KLAS Research, LLC. All Rights Reserved. NOTE: Performance scores may change significantly when including newly interviewed provider organizations, especially when added to a smaller sample size like in emerging markets with a small number of live clients. The findings presented are not meant to be conclusive data for an entire client base.