URGENT PRODUCT NOTIFICATION-EVD Sold Post 2018: The purpose of this letter is to advise you about a product sold after August 1, 2018. According to records, you received one or more of the following EVD products.
URGENT PRODUCT NOTIFICATION-EVD Sold 2014-2018: The purpose of this letter is to advise you about a product sold between August 1, 2014, and August 1, 2018. According to records, you received one or more of the following EVD products.
B. Braun Medical
RECALL-Rate Flow Regulator: This is to inform you that B. Braun Medical Inc. (BBMI) is issuing a voluntary medical device recall of Rate Flow® Regulator Administration sets due to reported deficiencies in the manufacturer’s quality systems at its manufacturing facility. Rate Flow Regulator Administration sets are manufactured by Leventon S.A.U. and purchased as a finished product by BBMI.
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