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October 26, 2006 Medical Device Recall AABB PulsePoints The Food and Drug Administration’s (FDA) Center for Biologics Evaluation and Research (CBER) has announced a medical device recall by Dupaco Inc. of Oceanside, Calif., for the Blood/Fluid Warming Set. According to the recall notice, the company has become aware of two leakage failures that have occurred in two warming sets out of approximately 12,000 distributed. Customers have been asked to contact the manufacturer to arrange for product return. DATE RECALL INITIATED: October 2006 PRODUCT: Dupaco Blood/Fluid Warming Set (No. D25480) LOT NUMBERS: 030603 To view CBER’s notice in its entirety, visit http://www.fda.gov/cber/recalls/dupaco101106.htm. -- End of AABB PulsePoints -- |
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Posted Oct. 26, 2006
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