Dermamedics, L.L.C. recalls Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics Post-Laser Treatment System with a SKU number of DM
Recalled August 6, 2014 · FDA recall D-1492-2014 · Dermamedics, L.L.C
Hazard
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded. · FDA Class II
Sold at
Nationwide
Description
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
Product
Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics Post-Laser Treatment System with a SKU number of DM 1019
Manufacturer(s)
Dermamedics, L.L.C.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →