Smiths Medical, a Minneapolis-based medical device-maker, is recalling its Medfusion syringe pumps after discovering a software issue that could cause the pumps’ low battery alarms to stop working.
The U.S. Food and Drug Administration on Wednesday gave Minnesota-made syringe infusion pumps a Class 1 recall classification, the most serious category of market withdrawals. The device is made by ...
(MENAFN- Techsci Research) Rising instances of chemotherapy for chronic disease treatment is driving the growth of United States Syringe Pumps Market, in the forecast period. According to TechSci ...
LONDON--(BUSINESS WIRE)--The global smart syringe pumps market is expected to post a CAGR of nearly 9% during the forecast period 2019-2023, according to the latest market research report by Technavio ...
FDA recently published a statement categorizing the recall of Cardinal Health Monoject single use Luer Lock Syringes (1, 6, 12, 20, 35, and 60mL) as Class I. The Monoject disposable syringes are used ...
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