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Harmless Harvest Inc.
Recall · Class II2017-10-30Terminated

May have spoiled, fermented or grown mould.

Recall of four varieties of Probiotic drinks due to premature spoilage. Testing has identified Candida lusitaniae as the predominate microorganism as the cause of spoilage.

Above, in the agency’s own words. The line before it is our plain-English summary — how we word these.

Issued by the US Food and Drug Administration, naming Harmless Harvest Inc..

What the notice covered

Harmless Coconut Probiotics Original; Coconut Cultured Beverage; UPC 859078-002542; Keep refrigerated 11 lf. oz. HDPE Bottle Ingredients: Organic Coconut Water, Water, Organic Coconut Meat, Organic Cane Sugar, live and active cultures. Harmless Harvest

Quoted from the record as published. If a product is not described here, this notice does not tell us whether it was affected.

What Class II means

The FDA’s middle class: use of the product may cause temporary or medically reversible health consequences, and the probability of serious harm is remote.

This is the agency’s own definition of the class. We do not assign classes and we do not rank them against each other.

The record

Agency
US Food and Drug Administration (FDA)
Reference number
F-0349-2018
Kind of action
Recall
Dated
2017-10-30
Terminated
2018-02-28
Status on the record
Terminated
We read it
2026-10-01

Regulates most packaged food, drugs and devices. Its recall records are published weekly in the Enforcement Report.

Products we matched to this notice

We have not matched this notice to any product in our database — usually because it named no barcode we hold. Products may still have been affected.

How we are treating it

This notice concerns the product line itself or how it was produced.

The government record

The FDA publishes this notice through its enforcement API, so the link below returns raw JSON rather than a readable page. It is the primary record and we cite it as such; everything above is our transcription of it.

https://api.fda.gov/food/enforcement.json?search=recall_number:"F-0349-2018"

To see it in the FDA’s own words, search the reference number F-0349-2018 in the Search the FDA Enforcement Report. The FDA publishes no direct link to an individual recall.

How we source every record on this site