Class IIOngoingVoluntary: Firm initiated

LIQUID BLENZ CORP: food recall H-0785-2026

LIQUID BLENZ CORP of Rockville Centre, NY recalled Pure Diabetes Bully 16 oz and 32 oz. Reason: May be under-processed resulting in growth of Clostridium botulinum and lists health claims. The FDA listed it as Class II in its Enforcement Report dated May 27, 2026; distribution: New York.

Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
Pure Diabetes Bully 16 oz and 32 oz.
Product quantity
18,190 bottles total
Reason for recall
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Codes, lots and dates on the package
16 oz with upc: 195893374878 & 32 oz with upc: 195893984466 Lots: DB58525, DB58885, DB21000, DB58661, DB25909, DB09550, DB66236, DB52855
Distribution pattern
NY and online sales
Recalling firm
LIQUID BLENZ CORP, Rockville Centre, NY
Classification
Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmApr 6, 2026
Classified by the FDAMay 18, 2026
Published in the Enforcement ReportMay 27, 2026

Other products in the same recall event

The FDA groups related products under one recall event (event 98765).

All food recall records

OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.

Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0785-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.