Z-1499-2014Class II

Mega-Gen His Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80708-3; Mega-Gen Hers Personal Lubricant, 8...

Name: Z-1499-2014 Mega-Gen His Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80708-3; Mega-Gen Hers Personal Lubricant, 8...
Creator: Altasource LLC dba Meta Labs LLC
Published: 2014-02-03
License: https://open.fda.gov/license/

Altasource LLC dba Meta Labs LLC / initiated 2014-02-03 / Open, Classified / root cause: manufacturing process

FDA source

Altasource LLC dba Meta Labs LLC began a recall of Mega-Gen His Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80708-3; Mega-Gen Hers Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80808-0 Product... on 2014-02-03. FDA classified it as Class II and gives the reason as "Firm is not registered as a drug manufacturer". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-1499-2014
Classification: Class II
Status: Open, Classified
Initiated: 2014-02-03
Posted: 2014-04-24
Recalling firm: Altasource LLC dba Meta Labs LLC
Product: Mega-Gen His Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80708-3; Mega-Gen Hers Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80808-0 Product Usage: A topical gel that increases sexual excitement and pleasure.
Product code: NA
Reason for recall: Firm is not registered as a drug manufacturer.
Root cause tag: manufacturing process
FDA 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 in commerce: 7
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.
Product codes and lots: Lot 8-94034

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1499-2014
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1498-2014	Class II	Ongoing	Voluntary: Firm initiated	2014-04-30	2014-04-24
Z-1499-2014	Class II	Ongoing	Voluntary: Firm initiated	2014-04-30	2014-04-24
Z-1500-2014	Class II	Ongoing	Voluntary: Firm initiated	2014-04-30	2014-04-24
Z-1501-2014	Class II	Ongoing	Voluntary: Firm initiated	2014-04-30	2014-04-24

Product code NA

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)