The FDA is spotlighting a new medical device correction effort at Baxter over its large-volume Novum IQ infusion pump, following reports of 79 serious injuries and two deaths linked to potential under ...
May 1, 2006 — The US Food and Drug Administration (FDA) has advised healthcare professionals of additional safety measures to consider when using Colleague volumetric infusion pumps (made by Baxter ...
DEERFIELD, Ill.--(BUSINESS WIRE)--Baxter International Inc. (NYSE:BAX), an innovative leader in infusion therapies and technologies, today announced U.S. Food and Drug Administration (FDA) 510(k) ...
LOS ANGELES (Reuters) - Baxter International Inc said on Monday it will recall its Colleague infusion pumps from the U.S. market on an order from the Food and Drug Administration under the company's ...
After a drawn-out approval process, medical equipment company Baxter International received regulatory clearance for a new infusion pump machine that is expected to help the company capture more of ...
To date, there have been no reports of serious injury associated with this issue. Baxter International has issued an Urgent Medical Device Correction for the Novum IQ syringe infusion pump due to the ...
Errors in the setup or management of some of Baxter International’s infusion pumps could result in overlooked blockages in the pumps, potentially leading to serious injury or even death, the ...
DEERFIELD - Baxter International Inc. said the Food and Drug Administration has granted medical device clearance for its new Novum IQ syringe infusion pump and related software. Syringe infusion pumps ...
LOS ANGELES, May 3 (Reuters) - Baxter International Inc said on Monday it will recall its Colleague infusion pumps from the U.S. market on an order from the Food and Drug Administration under the ...
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