Drug recall: Dermamedics Post Procedure Cream, 1 ounce containers which were distributed with a SKU number of DM 1026
FDA enforcement event 67247 is a drug recall by Dermamedics, L.L.C. of Oklahoma City, OK, initiated 10 Jan 2014 and classified Class II, with 9 product records.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 58% of the 313 drug enforcement events initiated in 2014 carry the same class.
Status: Terminated, terminated 14 Mar 2017. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Dermamedics, L.L.C..
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Dermamedics, L.L.C., Oklahoma City, OK.
Reason for recall
"Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded."
Distribution
"Nationwide"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| D-1487-2014 | Dermamedics Post Procedure Cream, 1 ounce containers which were distributed with a SKU number of DM 1026 | unknown | Class II | Terminated | 6 Aug 2014 |
| D-1488-2014 | Dermamedics Calm & Correct Cream in 2 oz. containers with SKU number DM1020. | unknown | Class II | Terminated | 6 Aug 2014 |
| D-1489-2014 | Dermamedics Baby's Relief Calm and Repair Cream in 2 oz. containers with a SKU number of DM1016 and 0.25 containers with a SKU number of PS 1016; and Therametics Baby's Relief Calm and Repair Cream in 2 oz. containers with a SKU number of BR008. | unknown | Class II | Terminated | 6 Aug 2014 |
| D-1490-2014 | Dermamedics Complexion Repair Topical Rehydrating Emulsion which was distributed in 50 ml containers with a SKU number of DM 1011 and Therametics Complexion Repair Topical Rehydrating Emulsion which was distributed in 50 ml containers with a SKU number of CR002. | unknown | Class II | Terminated | 6 Aug 2014 |
| D-1491-2014 | Dermamedics Calm and Correct Serum, 2 oz. containers with a SKU number of BB10062 and 4 oz. containers with a SKU number of BB10068. | — | Class II | Terminated | 6 Aug 2014 |
| D-1492-2014 | Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics Post-Laser Treatment System with a SKU number of DM 1019 | — | Class II | Terminated | 6 Aug 2014 |
| D-1493-2014 | Dermamedics Calm and Correct Cream 2 oz. containers in the Dermamedics Post Medical Procedure Kit with a SKU number of SK1005 | — | Class II | Terminated | 6 Aug 2014 |
| D-1494-2014 | Dermamedics Complexion Repair Topical Rehydrating Emulsion in 50 ml and 30 ml containers in the Dermamedics Complexion Repair Acne Treatment System Kit with SKU numbers of DM 1013 and DM 1025, respectively; Therametics Complexion Repair Topical Rehydrating Emulsion which was distributed in 50 ml containers with a SKU… | — | Class II | Terminated | 6 Aug 2014 |
| D-1495-2014 | Therametics Complexion Repair Topical Rehydrating Emulsion in 50 ml and 30 ml containers in the Complexion Repair Acne Treatment System Kit and the Complexion Repair Acne Travel Kit with SKU numbers of CR1005 and CR1007, respectively. | — | Class II | Terminated | 6 Aug 2014 |
Context
Questions and answers
Why was this drug recalled?
FDA's record gives the reason for recall as: "Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "Nationwide"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 14 Mar 2017. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA drug enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.