Liquid Blenz Soursop Bitters Recall Issued

Source: FDA · New York

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LIQUID BLENZ CORP is recalling Liquid Blenz Soursop Bitters due to potential under-processing that may allow growth of Clostridium botulinum.

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

This notice was issued by FDA on June 11, 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.

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

Which Products Are Affected The recall covers Liquid Blenz Soursop Bitters in 16 oz (UPC 860005735006) and 32 oz (UPC 860005735013) sizes. Affected lots are SS75223, SS00669, SS95811, SS95114, SS11139, SS54495, SS81258, and SS44886. 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. Contact information for returns or refunds is not provided in the recall notice.

Why This Matters The recall addresses a potential risk of Clostridium botulinum growth in the affected beverages distributed in New York and online.

Source FDA recall H-0782-2026, https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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 Liquid Blenz Soursop Bitters due to potential under-processing that may allow growth of Clostridium botulinum.
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.