Class IIOngoing · reported 2026-05-27

Pure Shilajit Tonic 16 oz and 32 oz

LIQUID BLENZ CORP recalled this product and the FDA reported the enforcement action on 27 May 2026 as Class II. The recall was initiated by the firm. May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product: Pure Shilajit Tonic 16 oz and 32 oz
Reason for recall: May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Recalling firm: LIQUID BLENZ CORP
Firm location: Rockville Centre, New York, United States
Classification: Class II
Status: Ongoing
Recall number: H-0791-2026
Quantity: 18,190 bottles total
Distribution: NY and online sales
Initiated: 6 April 2026
Reported by FDA: 27 May 2026
Firm notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product codes: 16 oz with upc: 860010984482 & 32 oz with upc: 860010984499 Lots: not provided

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
This is one of 13 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 13 separate recalls, which almost every published figure does, overstates it by a factor of 13. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 13 of them.
This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
The distribution pattern names 1 state, and the FDA published the enforcement report 7 weeks after the firm began the recall.
The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.

What this recall was for

Process deviation

A process deviation recall means the process ran outside its validated limits: a thermal process that did not reach its time and temperature, a pH that drifted, or a seal that failed.

A preventive controls plan covers a process deviation under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.

21 CFR 113: Thermally processed low-acid foods in hermetically sealed containers: the scheduled process, its establishment by a competent authority, and the records proving every container received it.
21 CFR 114: Acidified foods: the controls on equilibrium pH at or below 4.6, and the process that achieves it.
21 CFR 117.150: Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.

Clostridium botulinum

Clostridium botulinum recalls are recalls of the process, not of a test result: the organism produces its toxin without oxygen, so a low-acid food in a sealed container that missed its scheduled process is recalled whether or not toxin was ever found.

A preventive controls plan covers a botulism risk under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.

21 CFR 113: Thermally processed low-acid foods in hermetically sealed containers: the scheduled process, its establishment by a competent authority, and the records proving every container received it.
21 CFR 108.35: Emergency permit control: the registration and process filing a low-acid canned food processor must hold before it may operate.

Other records from LIQUID BLENZ CORP

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 12 other records name this firm.

Reported	Product	Firm	Reason	Class
2026-05-27	Menopause Bully 16 oz and 32 oz.	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II
2026-05-27	Fibroid Bully 16 oz and 32 oz.	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II
2026-05-27	Prostate Bully 16 oz and 32 oz	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II
2026-05-27	Blackseed Bitters 16 oz and 32 oz.	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II
2026-05-27	Immunity Enhancer Elderberry 16 oz and 32 oz.	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II
2026-05-27	Liquid Blenz Good Brain Tonic 16 oz and 32 oz	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II
2026-05-27	Pure Diabetes Bully 16 oz and 32 oz.	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II
2026-05-27	Liquid Blenz Soursop Bitters 16 oz and 32 oz.	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II
2026-05-27	Flat Belly Bully 16 oz and 32 oz	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II
2026-05-27	Sea Moss Tonic 16 oz and 32. oz.	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II

All 13 records for LIQUID BLENZ CORP

All 2026 recalls · All FDA food recall data

21 CFR 113 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.