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American Beverage Corporation
Recall · Class II2012-05-15Terminated

There is a possibility that a part of the nozzle cap of the bottle can become dislodged through abuse (i.e. excessive chewing), and then possibly ingested, posing a potential health/safety hazard. The cap in question is no longer used by ABC and was last produced in September of 2011. Firm does not anticipate finding any impacted product in the market.

Issued by the US Food and Drug Administration, naming American Beverage Corporation.

What the notice covered

Big Hug, Fruit Barrel Orange in a plastic 16 oz bottle with a sports cap, American Beverage Corp., Verona, PA.

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-0189-2014
Kind of action
Recall
Dated
2012-05-15
Terminated
2014-05-15
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-0189-2014"

To see it in the FDA’s own words, search the reference number F-0189-2014 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