The Recall Desk
ModerateFDA (Devices)·Z-1501-2014·Announced 2014-04-30

Meta Labs Recalls Hot Ice Topical Gel Due to Unregistered Manufacturer

Altasource LLC dba Meta Labs LLC is recalling 155 units of Hot Ice topical 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 hospitalizations. The primary issue is a regulatory compliance failure (unregistered manufacturer) rather than a direct physical hazard like contamination or defect, fitting the criteria for a moderate severity voluntary or compliance-driven recall.

Plain-English summary

Altasource LLC dba Meta Labs LLC is recalling 155 units of Hot Ice, 1 fl. oz. topical gel. The product is described as a gel intended to increase sexual excitement and pleasure. The recall is being conducted because the firm is not registered as a drug manufacturer.

The affected product is identified by Lot 8-94034 and UPC 80705-2. The recall covers distribution in the United States, specifically in the states of 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 who have purchased this product should stop using it and contact the recalling firm for further instructions. The recall is classified as Class II by the FDA.

The recalled product

Product
Hot Ice, 1 fl. oz., Meta Labs LLC, UPC 80705-2 Product Usage: A topical gel that increases men and womens secual excitement and pleasure.
Manufacturer
Altasource LLC dba Meta Labs LLC
Category
Drug — Topical Gel
Hazard
Affected units
155

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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