CLASS II ONGOING Drug recall · Reported 19 Apr 2017 · FDA Enforcement Report
Double Hyaluronic 1000, 'AN Ounce OF Gold' Volumizing Day recalled
Signature Club A is recalling Double Hyaluronic 1000, 'AN Ounce OF Gold' Volumizing Day Cream, Broad Spectrum Spf 30+, distributed nationwide in the US. The recall was initiated on 1 Mar 2017 and the FDA has classified it as Class II.
Check your package
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-0662-2017
- FDA event ID
- 76714
- Recalling firm
- Signature Club A, Tampa, FL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 1 Mar 2017
- FDA classified
- 12 Apr 2017
- Reported
- 19 Apr 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Sterility
- Drug class
- Creams, Ointments & Gels
Timeline
| 1 Mar 2017 | Recall initiated by company | |
| 12 Apr 2017 | Classified by FDA | +42 days |
| 19 Apr 2017 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Microbial Contamination of Non-Sterile Products: odor complaint of product due to microbial contamination.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Double Hyaluronic 1000, 'AN OUNCE OF GOLD' Volumizing Day Cream, Broad Spectrum SPF 30+, (Octinoxate 7.725%, Oxybenzone 6.18%, Octisalate 5.15%, Avobenzone 3.09%), Net Wt. 1.8 oz. (51 g) jar, Distributed by Signature Club A, Ltd, Tampa, FL 33609.
Where it was distributed
Nationwide in the USA
Questions about this recall
Why was it recalled?
Microbial Contamination of Non-Sterile Products: odor complaint of product due to microbial contamination.
Which lots are affected?
Lot #: 1626253/1746. Exp 10/18
Where was it sold?
Nationwide in the USA
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.