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Use caution Drug recall · FDA · Published March 1, 2017

Signature Club A Recalls Double Hyaluronic 1000 Cream Due to Contamination

Signature Club A Ltd recalls Double Hyaluronic 1000 cream due to microbial contamination. Check lot numbers and expiration dates for affected jars.

🇺🇸 FDA recall #D-0662-2017DrugSignature Club A ›
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Recalling firmSignature Club A Ltd550 N Reo St Ste 300 · Tampa, FL 33609-1037
✎ GovInfoNow plain-language explainer

What happened, in plain English

Signature Club A Ltd is recalling Double Hyaluronic 1000 'AN OUNCE OF GOLD' Volumizing Day Cream because of microbial contamination that caused an odor complaint. The recall affects 1,237 jars distributed nationwide in the USA. The record does not specify a remedy or return process for consumers. Read more at govinfonow.com/recall/41861-signature-club-a-recalls-double-hyaluronic-1000-cream-due-to.

Source Summary by GovInfoNow · govinfonow.com/recall/41861-signature-club-a-recalls-double-hyaluronic-1000-cream-due-to · Updated October 11, 2026 · FDA enforcement record: FDA #D-0662-2017

Cite this page

“Signature Club A Recalls Double Hyaluronic 1000 Cream Due to Contamination.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/41861-signature-club-a-recalls-double-hyaluronic-1000-cream-due-to. Based on FDA recall #D-0662-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0662-2017%22&limit=1).

Why it’s dangerous

The product was found to have microbial contamination, which resulted in an unpleasant odor. While the record does not detail specific injuries, using contaminated non-sterile skincare products can potentially lead to skin irritation or infection.

Who’s affected

Consumers in the USA who purchased this specific volumizing day cream from Signature Club A Ltd between its production and the recall date of March 1, 2017. Individuals with sensitive skin or compromised immune systems may be at higher risk from microbial exposure.

How to tell if you have this one

Look for a 1.8 oz (51 g) jar of 'AN OUNCE OF GOLD' Volumizing Day Cream with Broad Spectrum SPF 30+. Check the lot number, which must be 1626253/1746, and verify the expiration date is 10/18.

  • Brand
    Signature Club A
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not apply the cream to your skin if you have a jar matching the recalled lot number.

  2. Check your lot number

    Verify that your jar has lot number 1626253/1746 and an expiration date of 10/18.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 49 days after the firm started it.

1. Firm started the recall: Mar 1, 201712. FDA classified it Class II: Apr 12, 201723. Published in FDA’s Enforcement Report: Apr 19, 201732017
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0662-2017 (March 1, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0662-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA