Recall Notification to Clients with Possible Product On-Hand, Effective 9/28/18
DATE RECALL INITIATED:
September 28, 2018
PRODUCT / LOT NUMBER:
ALL ReGen Series
San Diego, CA
Yorba Linda, CA
Consignees were instructed to not use the vials, due to reported adverse reactions.
Liveyon will be coordinating product return for a full refund.
The information in this listing reflects CBER's best efforts to communicate information that has been reported to FDA. Its accuracy and comprehensiveness cannot be guaranteed.