Product Safety Recalls

Product Recall Tracker

Recall D-0451-2023

Description: Activator Concentrate (sodium fluoride 0.96% in Activator) 1 fl. Oz, liquid oral rinse plastic bottles, Manufactured for: All USA Direct LLC, Broadview, IL 60155

Recall D-0451-2023 Information

Mandated?Voluntary: Firm initiated
Recall NumberD-0451-2023
Event ID91719
DistributionNationwide within the United States
Quantity34,320 bottles
Drug ClassificationClass II
Drug Code Info20230315
Recall Initiation Date20230224
Report Date20230315
Classification Date20230308
Address19 Concord St
Norwalk, CT 06854-3706
United States
Recalling FirmEcometics, Inc.
Initial Notification Letter
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