CLASS II ONGOING Device recall · Reported 30 Apr 2014 · FDA Enforcement Report
Mega-Gen His Personal Lubricant, Meta Labs recalled by Altasource
Altasource is recalling Mega-Gen His Personal Lubricant, Meta Labs, 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
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-1499-2014
- 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
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.
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 ArkansasArizonaCaliforniaColoradoFloridaGeorgiaIdahoIllinoisKentuckyLouisianaMichiganNorth CarolinaNebraskaNevadaNew YorkOhioPennsylvaniaTennesseeTexasUtah
Questions about this recall
Is Mega-Gen His Personal Lubricant, Meta Labs recalled?
Yes. Altasource recalled Mega-Gen His Personal Lubricant, Meta Labs on 3 Feb 2014. The recall is Class II and its status is Ongoing. Recall number Z-1499-2014.
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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