FDA MedWatch - 53 Nutritional and Beverage Products by Lyons Magnus

Recall - Due To The Potential For Microbial Contamination

If your email program has trouble displaying this email, view as a webpage. MedWatch - The FDA Safety Information and Adverse Event Reporting Program TOPIC: 53 Nutritional and Beverage Products by Lyons Magnus: Recall - Due To The Potential For Microbial Contamination AUDIENCE: Consumer, Patient, Health Professional, Pharmacy ISSUE: Lyons Magnus LLC is recalling nutritional and beverage products due to the potential for microbial contamination, including from the organism Cronobacter sakazakii. The list of recalled products does not include products intended for infants (i.e. under the age of one). While infection related to Cronobacter sakazakii is rare, the common symptoms of illness could include fever, vomiting and urinary tract infection. However, vulnerable and immunocompromised populations may be more susceptible to infection. Preliminary root cause analysis shows that the products did not meet commercial sterility specifications. To date, no illnesses or complaints related to these products have been reported. The recalled products should not be consumed. For more information about this recall, click on the red button "Read Recall" below. BACKGROUND: The products being recalled are sold as nutritional and beverage products. RECOMMENDATIONS:  Anyone who has a recalled product in his or her possession should dispose of it immediately or return it to the place of purchase for a refund. If you are a consumer, health professional, or member of the food industry who wants to voluntarily report a complaint or adverse event (illness or serious allergic reaction) related to a food product, you have two choices: Call an FDA Consumer Complaint Coordinator if you wish to speak directly to a person about your problem. Report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program: Complete and submit the report online. Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on form, or submit by fax to 1-800-FDA-0178. Follow us on Twitter at @FDAMedWatch

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