Overview of recall records associated with Koogee-Queen Anne, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 87.
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
This page summarizes recall records in which the official source identifies Koogee-Queen Anne, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
