The Recall Desk
ModerateFDA (Devices)·Z-1498-2014·Announced 2014-04-30

FDA Recalls Amo-O Herbal Stimulator Gel for Unregistered Manufacturer

Altasource LLC is recalling 70 units of Amo-O Herbal Stimulator gel because the firm is not registered as a drug manufacturer.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, but the source text does not report any illnesses, injuries, or specific health hazards, only a regulatory registration deficiency. This aligns with the rubric for moderate severity involving regulatory or labeling issues without reported harm.

Plain-English summary

Altasource LLC dba Meta Labs LLC is recalling 70 units of Amo-O Herbal Stimulator, a 2 fl. oz. nonprescription topical gel. The product is manufactured by Meta Labs in Alpharetta, GA, and is used to enhance libido and stimulate orgasmic pleasure.

The recall was initiated because the firm is not registered as a drug manufacturer. The affected product is identified by Lot 8-94034 and UPC Code 80702-1.

The product was distributed nationwide in Arizona, Arkansas, California, Colorado, Florida, Georgia, Idaho, Illinois, Kentucky, Louisiana, Michigan, Nebraska, Nevada, New York, North Carolina, Ohio, Pennsylvania, Tennessee, Texas, Utah, and Virginia. Consumers should stop using the product and contact the recalling firm for instructions.

The recalled product

Product
Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The product is a nonprescription, topical gel that is used to enhance libido and stimulate orgasmic pleasure.
Manufacturer
Altasource LLC dba Meta Labs LLC
Category
Drug — Topical Gel
Hazard
Affected units
70

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot 8-94034

Distribution

Distributed nationwide across the United States.

The notice also names 21 states specifically:

Part of a larger recall action

This product is one of 4 recalled by Altasource LLC dba Meta Labs LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 4 products in this recall →

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