dr. brandt, BB cream with signature FLEXITONE, SPF 30, 1 oz./30 g tube, Distributed by: Cosmetic Dermatology, Inc., Miami, FL 33172, UPC 6 63963 00828 7.

Recall Insight

This FDA Drug action (record #D-0065-2019) was formally reported on October 24, 2018, with the manufacturer initiating the action on August 3, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Product Quest Manufacturing LLC is listed as the recalling firm, operating out of Daytona Beach, FL. Federal records indicate 9,480 tubes units are affected.

The documented reason for this recall is: Failed Stability Specifications: separation of product and failure for actives. Distribution data in the federal record shows the product reached: Nationwide in the USA. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 4 were also issued by FDA Drug. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 8 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.