FDA Device recall Z-1498-2014
Amo-O Herbal Stimulator, 2 fl. oz
- FDA Device
- Class II
- ongoing
- Published 2014-04-30
On 2014-04-30 the FDA classified a Class II recall of Amo-O Herbal Stimulator, 2 fl. oz by Altasource, citing firm is not registered as a drug manufacturer.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1498-2014 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2014-02-03 |
| Published | 2014-04-30 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Altasource |
| Distribution | US |
Product
Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The product is a nonprescription, topical gel that is used to enhance libido and stimulate orgasmic pleasure.
Reason
Firm is not registered as a drug manufacturer.
Identifiers
| code_info | Lot 8-94034 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1498-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.