The nonprofit medtech research group ECRI Institute dubbed a B. Braun infusion pump "fair," prompting the company to question ECRI's testing methods. Nancy Crotti B. Braun Medical has accused the ECRI ...
The Food and Drug Administration has categorized B. Braun Medical’s correction of infusion pumps as a Class I event. B. Braun contacted customers in September about faulty occlusion alarms that can ...
For the fourth time already this month, the FDA has issued a notice formally bestowing a Class I label—denoting a heightened risk of serious injury or death—upon a recall of yet another drug delivery ...
FILE PHOTO: Signage is seen outside of FDA headquarters in White Oak, Maryland (Reuters) - The U.S. Food and Drug Administration (FDA) on Friday said it had identified the recall of B. Braun Medical ...
McAfee Enterprise's Advanced Threat Research Team has unveiled a new study about vulnerabilities they found with pumps created by German healthcare giant B. Braun. The report chronicles the problems ...
Drug delivery devices are in the safety regulation crosshairs as of late, as a growing list of the technologies have found themselves the subject of recalls and corrections in recent weeks. Latest to ...
Security vulnerabilities are found to be a nuisance for the healthcare industry. Many medical devices, such as ultrasounds, mammography machines, pacemakers, and other equipment can be easily ...
McAfee Enterprise’s Advanced Threat Research Team released new findings about vulnerabilities in the B. Braun Infusomat Space Large Volume Pump and the B. Braun SpaceStation, both of which are ...
February 2, 2011 — The US Food and Drug Administration (FDA) has issued a class I recall for units of the Outlook 400ES Safety Infusion System (B. Braun). A software update may cause normal operation ...
LONDON--(BUSINESS WIRE)--Technavio has been monitoring the global programmable infusion pumps market and the market is poised to grow by USD 487.81 million during 2020-2024 at a CAGR of almost 8% ...
B. Braun Medical Inc. (B.Braun), a leader in infusion therapy and pain management, has received 510(k) clearance for its second-generation, large-volume Infusomat Space Pump. The Infusomat Space Pump ...
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