The recently released Consumer Reports’ Hospital Ratings of more than 1,000 U.S. hospitals highlighted the need to reduce hospital-caused patient harm. On a safety scale with 100 being the highest, ...
October 18, 2010 — A class 1 recall of CareFusion's Alaris point of care units (PC units), model 8015, has been issued, the US Food and Drug Administration (FDA) announced October 15. The device is a ...
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 ...
DEERFIELD, Ill.--(BUSINESS WIRE)--Baxter International Inc. (NYSE:BAX), a leader in innovative technology for medication delivery, announced new data from a retrospective study finding that machine ...
April 14, 2011 — Moog Inc's voluntary recall of certain ambulatory infusion pumps has now been upgraded to a class 1 recall by the US Food and Drug Administration (FDA), the company and the agency ...
The FDA gave 510(k) clearance to Smiths Medical's "smart" infusion pump, which includes error-prevention software for a number of therapies. The company says its CADD-Solis VIP pump improves on the ...
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