LIQUID BLENZ CORP Recalls Blackseed Bitters

Source: FDA · New York

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LIQUID BLENZ CORP is recalling 18,190 bottles of Blackseed Bitters due to potential under-processing that may allow Clostridium botulinum growth.

What this FDA recall tells you, and what most readers miss

This notice was issued by FDA on June 10, 2026 and geographically references New York. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.

Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to read it as a data point about the issuing system: how quickly FDA detected the hazard, how precise the geographic or product-identifier scope is, and whether similar notices have clustered in the same category or region in the last 90 days. Cluster patterns frequently precede a broader regulatory action, a single localized FDA recall is isolated; three of them within a quarter often indicate a supply-chain, infrastructure, or seasonal driver that will keep producing notices until something structural changes.

For decision-making, Areazine pairs each alert with the original agency URL, the full agency name, and a timestamp so you can verify the notice against the primary source before acting on it. Tags on this item (recall, product-safety, fda, Food) map to related alerts in the same area of risk - browsing them together gives a clearer picture than any single notice alone, because the shape of an ongoing issue only becomes visible across multiple sequential alerts.

What Happened

LIQUID BLENZ CORP initiated a voluntary recall of Blackseed Bitters because the products may be under-processed, resulting in potential growth of Clostridium botulinum, and list health claims.

Which Products Are Affected

The recall covers Blackseed Bitters in 16 oz (UPC: 860005735020) and 32 oz (UPC: 860005735037) sizes. Affected lots are BS62367, BS25400, BS11595, BS75444, BS75721, BS90605, and BS34888. A total of 18,190 bottles are affected. Distribution was limited to NY and online sales.

What You Should Do

Consumers should not consume the recalled products.

Why This Matters

The recall involves a potential risk of Clostridium botulinum growth in food products distributed in New York and online.

Source

FDA recall number H-0783-2026 (Class II, ongoing).

Original source: FDA Official Notice ↗

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Frequently Asked Questions

Common questions about this FDA recall.

What is this FDA recall about?
LIQUID BLENZ CORP is recalling 18,190 bottles of Blackseed Bitters due to potential under-processing that may allow Clostridium botulinum growth.
Which agency issued this alert?
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How severe is this alert?
This alert is classified as "medium" severity. Stay informed and follow agency guidance.
What area is affected?
This alert affects New York. Check with FDA for the most current geographic scope.
Where can I find more FDA Recalls updates?
Browse the full FDA Recalls feed on Areazine at areazine.com/recalls/fda/ for the latest updates from FDA and other agencies.