Double Hyaluronic 1000 — Class II drug recall D-0662-2017
Ongoing recall by Signature Club A Ltd, reported 2017-04-19, distributed nationwide. Microbial Contamination of Non-Sterile Products: odor complaint of product due to microbial contamination.
| Recall number | D-0662-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Signature Club A Ltd, Tampa, FL, United States |
| Recall initiated | 2017-03-01 |
| Classified | 2017-04-12 |
| Reported by FDA | 2017-04-19 |
| Distributed | Nationwide (US) |
| Quantity | 1,237 jars |
| Reason classes | microbial contamination, sterility |
| Lot numbers | 10/18, 1626253/1746 |
Product
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.
Reason for recall
Microbial Contamination of Non-Sterile Products: odor complaint of product due to microbial contamination.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0662-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.