Liquid Blenz Corp Recall History
Liquid Blenz Corp has had 1 FDA-tracked food recall since 2026. The full list below — sourced from the FDA openFDA enforcement database — shows dates, products, reasons, and classifications for every recall on record.
Key Facts
- Total Recalls
- 1
- Years in FDA Data
- Since 2026
- Class I (Most Serious)
- 0
- Most Common Reason
- N/A
- Latest Recall
- Apr 6, 2026
- First Recorded Recall
- Apr 6, 2026
- States Affected
- NY
- Currently Active
- 1
- Data Source
- FDA openFDA + USDA FSIS
Get recall alerts for Liquid Blenz Corp
We'll email you the moment Liquid Blenz Corp has a new FDA food recall. No spam — only real recalls.
Complete Recall List (1 Records)
Every Liquid Blenz Corp recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.
| Date | Product | Class | Status |
|---|---|---|---|
| Apr 6, 2026 | Menopause Bully 16 oz and 32 oz. | Class II | Active |
Recall data sourced from the FDA's recalls and safety alerts database. Class I recalls indicate a reasonable probability of serious adverse health consequences. Always check the USDA FSIS recall list for meat and poultry products.
Frequently Asked Questions
Yes, Liquid Blenz Corp has 1 FDA food recall on record, including 0 Class I (dangerous) recalls. There is currently 1 active recall.
Liquid Blenz Corp currently has 1 active recall. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.
Liquid Blenz Corp's 1 recall break down by severity: 0 Class I (may cause serious health issues), 1 Class II (may cause temporary health problems), and 0 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
Liquid Blenz Corp recalls have affected NY. Check individual recall entries for specific distribution details.
Related
Recall data is sourced from the FDA openFDA enforcement database. Classifications reflect FDA severity ratings: Class I (dangerous), Class II (may cause temporary health problems), Class III (unlikely harmful).
For this entity, the underlying data on this page comes from the FDA openFDA enforcement-report API. The breakdown above is the federal record; the paragraphs below add the per-entity context that makes the headline numbers usable for a real decision rather than just a data lookup.
Every number on this page links back to the FDA openFDA enforcement-report API; the methodology page describes the inputs, refresh cadence, and known limitations of the underlying data product.
Practical use of this page is in combination with the comparison and ranking pages elsewhere on the site, which surface the same data for this entity’s peers within U.S. consumer-product recalls. A single-entity reading without peer context can be misleading when an entity is an outlier on one axis but typical on another.