CLASS II Drug recall · Reported 6 Aug 2014 · FDA Enforcement Report

Therametics Complexion Repair Topical Rehydrating Emulsion recalled

Dermamedics is recalling Therametics Complexion Repair Topical Rehydrating Emulsion in and containers in the, distributed nationwide in the US. The recall was initiated on 10 Jan 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesall lot codes 30 ml and 50 ml

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1495-2014
FDA event ID
67247
Recalling firm
Dermamedics, Oklahoma City, OK
Classification
Class II
Status
Terminated
Recall initiated
10 Jan 2014
FDA classified
29 Jul 2014
Reported
6 Aug 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Labeling Errors

Timeline

10 Jan 2014Recall initiated by company
29 Jul 2014Classified by FDA+200 days
6 Aug 2014Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.

Product as listed by the FDA

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.

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.

Which lots are affected?

all lot codes 30 ml and 50 ml

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

8 other products · FDA event 67247

This product is part of a recall event; the main page for the event is Post Procedure Cream containers which were distributed recalled.

More recalls from Dermamedics

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