CLASS II ONGOING Device recall · Reported 30 Apr 2014 · FDA Enforcement Report

Hot Ice, Meta Labs LLC recalled by Altasource

Altasource is recalling Hot Ice, Meta Labs LLC, distributed nationwide in the US. The recall was initiated on 3 Feb 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 8-94034

Quantity recalled155

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1501-2014
FDA event ID: 67976
Recalling firm: Altasource, Roswell, GA
Classification: Class II
Status: Ongoing
Recall initiated: 3 Feb 2014
FDA classified: 24 Apr 2014
Reported: 30 Apr 2014
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

3 Feb 2014	Recall initiated by company
24 Apr 2014	Classified by FDA	+80 days
30 Apr 2014	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Firm is not registered as a drug manufacturer.

Product as listed by the FDA

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.

Where it was distributed

USA Nationwide in the states of AZ, AR, CA, CO, FL, GA, ID, IL,KY, LA, MI, NE, NV, NY, NC, OH, PA, TN, TX, UT, and VA.

Nationwide Arkansas Arizona California Colorado Florida Georgia Idaho Illinois Kentucky Louisiana Michigan North Carolina Nebraska Nevada New York Ohio Pennsylvania Tennessee Texas Utah

Questions about this recall

Is Hot Ice, Meta Labs LLC recalled?

Yes. Altasource recalled Hot Ice, Meta Labs LLC on 3 Feb 2014. The recall is Class II and its status is Ongoing. Recall number Z-1501-2014.

Why was it recalled?

Firm is not registered as a drug manufacturer.

Which lots are affected?

Lot 8-94034

Where was it sold?

USA Nationwide in the states of AZ, AR, CA, CO, FL, GA, ID, IL,KY, LA, MI, NE, NV, NY, NC, OH, PA, TN, TX, UT, and VA.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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