JOHNSON & JOHNSON MAXXUS SURGICAL GLOVE REACTION COMPLAINTS
This article was originally published in The Gray Sheet
Executive Summary
JOHNSON & JOHNSON MAXXUS SURGICAL GLOVE REACTION COMPLAINTS were not reported to the agency under the medical device reporting regulations, FDA charges in a Feb. 18 warning letter to the firm. Due to the unsubmitted reports, FDA considers the orthopedic latex surgical gloves, manufactured by Johnson & Johnson Medical in Arlington, Texas, misbranded.
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