RecallHawk
Class II Recall

Liquid Blenz Soursop Bitters 16 oz and 32 oz.

LIQUID BLENZ CORP

Summary

The FDA issued a Class II for Liquid Blenz Soursop Bitters 16 oz and 32 oz. by LIQUID BLENZ CORP. Reason: May be under-processed resulting in growth of Clostridium botulinum and lists health claims..

Details

Source

Food Recall

External ID

H-0782-2026

Action Date

2026-05-27

Status

Ongoing

Category

food

Product Description

Liquid Blenz Soursop Bitters 16 oz and 32 oz.

Lot/Code Info: 16 oz with upc: 860005735006 & 32 oz with upc: 860005735013 Lots: SS75223, SS00669, SS95811, SS95114, SS11139, SS54495, SS81258, SS44886

Quantity Affected: 18,190 bottles total

Reason for Recall

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

Distribution

NY and online sales

Type: Voluntary: Firm initiated

Recall Initiated: 2026-04-06

Company

LIQUID BLENZ CORP

Rockville Centre, NY

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 80 food recalls issued in the same week, part of 204 food-related FDA actions this month.

LIQUID BLENZ CORP has 13 FDA actions in our database, including 13 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (LIQUID BLENZ CORP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does LIQUID BLENZ CORP have FDA actions?

LIQUID BLENZ CORP has 13 FDA actions in our database, including 13 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0782-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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