FDA Medical Device Recalls (openFDA)
Altasource LLC dba Meta Labs LLC: 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.
- Recall number
- Z-1501-2014
- Recalling firm
- Altasource LLC dba Meta Labs LLC
- 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.
- Status
- Open, Classified
- Initiated
- 2014-02-03
- Posted
- 2014-04-24
- Terminated
- not on file
- Reason
- Firm is not registered as a drug manufacturer.
- Root cause
- No Marketing Application
- Action
- Meta Labs notified customers of the Voluntary Recall Notification letter on February 4, 2014. The letter requested that the products be returned. For questions call 770-645-0602.
- Quantity
- 155
- Distribution
- 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.
- Lot, serial or model codes
- Lot 8-94034
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- NA
- Firm FEI
- 3006271709
- Firm city
- Roswell
- Firm state
- GA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28