FDA recall H-0786-2026 · May 27, 2026
LIQUID BLENZ CORP: Pure Libido Drink 16 oz and 32 oz recall
Product
Pure Libido Drink 16 oz and 32 oz.
Reason for recall
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- 16 oz with upc: 195893463176 & 32 oz with upc: 195893949991 Lots: LB08560, LB18863, LB76882, LB84633, LB55881
- Quantity
- 18,190 bottles total
- Distribution
- NY and online sales
- Recalling firm
- LIQUID BLENZ CORP, Rockville Centre, NY
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-04-06
Source: openFDA enforcement record H-0786-2026 · search recall number H-0786-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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