CLASS II ONGOING Food recall · Reported 27 May 2026 · FDA Enforcement Report

Menopause Bully recalled by Liquid Blenz

Liquid Blenz is recalling Menopause Bully, distributed in New York. The recall was initiated on 6 Apr 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes16oz with upc: 860010984420 & 32oz with upc: 860010984437 Lots: not provided
Quantity recalled18,190 bottles total

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-0788-2026
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
Other

Timeline

6 Apr 2026Recall initiated by company
18 May 2026Classified by FDA+42 days
27 May 2026Published 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

Menopause Bully 16 oz and 32 oz.

Where it was distributed

NY and online sales

New York

Stores named: Online Retailers

Questions about this recall

Why was it recalled?

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Which lots are affected?

16oz with upc: 860010984420 & 32oz with upc: 860010984437 Lots: not provided

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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

12 other products · FDA event 98765

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