CLASS III Food recall · Reported 11 May 2016 · FDA Enforcement Report

Suma Root, www.iowaselectherbs.com, Cedar Rapids, IA recalled

Iowa Select Herbs is recalling Iowa Select Herbs LLC, Suma Root, www.iowaselectherbs.com, Cedar Rapids, IA 52402, distributed nationwide in the US. The recall was initiated on 11 Sep 2015 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot-21035 Expires-02/2019
Quantity recalled3 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1226-2016
FDA event ID
72083
Recalling firm
Iowa Select Herbs, Cedar Rapids, IA
Brand
Iowa
Classification
Class III
Status
Terminated
Recall initiated
11 Sep 2015
FDA classified
2 May 2016
Reported
11 May 2016
Type
FDA Mandated
Customers notified by
Press Release
Reason category
Labeling Errors
Product category
Other

Timeline

11 Sep 2015Recall initiated by company
2 May 2016Classified by FDA+234 days
11 May 2016Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.

Product as listed by the FDA

Iowa Select Herbs LLC, Suma Root, www.iowaselectherbs.com, 1 gallon, Cedar Rapids, IA 52402

Where it was distributed

The recalled product was distributed to retail stores in CA, FL, GA, IA, MI, MO, MT, NY, and SC and consumers nationwide and internationally in Denmark, Canada, UK, Australia, and Serbia.

Nationwide CaliforniaFloridaGeorgiaIowaMichiganMissouriMontanaNew YorkSouth Carolina

Questions about this recall

Is Suma Root, www.iowaselectherbs.com, Cedar Rapids, IA 52402 recalled?

Yes. Iowa Select Herbs recalled Suma Root, www.iowaselectherbs.com, Cedar Rapids, IA 52402 on 11 Sep 2015. The recall is Class III and its status is Terminated. Recall number F-1226-2016.

Why was it recalled?

Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.

Which lots are affected?

Lot-21035 Expires-02/2019

Where was it sold?

The recalled product was distributed to retail stores in CA, FL, GA, IA, MI, MO, MT, NY, and SC and consumers nationwide and internationally in Denmark, Canada, UK, Australia, and Serbia.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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