CLASS II ONGOING Food recall · Reported 27 May 2026 · FDA Enforcement Report
Pure Libido Drink recalled by Liquid Blenz
Liquid Blenz is recalling Pure Libido Drink, distributed in New York. The recall was initiated on 6 Apr 2026 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0786-2026
- FDA event ID
- 98765
- Recalling firm
- Liquid Blenz, Rockville Centre, NY
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 6 Apr 2026
- FDA classified
- 18 May 2026
- Reported
- 27 May 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Botulism
- Product category
- Sexual Enhancement Products
Timeline
| 6 Apr 2026 | Recall initiated by company | |
| 18 May 2026 | Classified by FDA | +42 days |
| 27 May 2026 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Product as listed by the FDA
Pure Libido Drink 16 oz and 32 oz.
Where it was distributed
NY and online sales
Stores named: Online Retailers
Questions about this recall
Is Pure Libido Drink recalled?
Yes. Liquid Blenz recalled Pure Libido Drink on 6 Apr 2026. The recall is Class II and its status is Ongoing. Recall number H-0786-2026.
Why was it recalled?
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Which lots are affected?
16 oz with upc: 195893463176 & 32 oz with upc: 195893949991 Lots: LB08560, LB18863, LB76882, LB84633, LB55881
Where was it sold?
NY and online sales
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
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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