Rootify
CompaniesFAQ
Schwabe North America Inc.
Recall · Class II2013-10-23Terminated

May contain a chemical that should not be in it.

Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic chloramphenicol.

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 Schwabe North America Inc..

What the notice covered

Nature's Way,UPC 33674156797, Alive Once Daily MultiVitamin Ultra Potency, 60 Tabs, 20008123, 20010552

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-0836-2014
Kind of action
Recall
Dated
2013-10-23
Terminated
2015-02-26
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-0836-2014"

To see it in the FDA’s own words, search the reference number F-0836-2014 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