PlainRecalls
LowClass IIITerminated

FDA Food recall · Reported May 11, 2016

Iowa Select Herbs LLC, Burdock Root, www.iowaselectherbs.com, 4 fl. Oz.., Cedar Rapids, IA 52402

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 …

Recall #
F-1154-2016
Affected scope
24 bottles
Initiated
September 11, 2015
Verify with FDA Food →
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Iowa Select Herbs LLC recalled Iowa Select Herbs LLC, Burdock Root, www.iowaselectherbs.com, 4 fl. Oz.., Cedar Rapids, I… - a low-severity action.

Iowa Select Herbs LLC, Burdock Root, www.iowaselectherbs.com, 4 fl. Oz.., Cedar Rapids, I… was recalled by Iowa Select Herbs LLC in May 11, 2016. Reason: Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products beca…. Check the official notice for the remedy. Verify recall #F-1154-2016 with the FDA Food before acting.

The recall

Iowa Select Herbs LLC issued this low-severity FDA Food recall-Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products beca….

Low
severity level
Class III
classification
May 11, 2016
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1154-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-1154-2016) was formally reported on May 11, 2016, with the manufacturer initiating the action on September 11, 2015. It is classified under Low severity (Class III), with a current status of Terminated. Iowa Select Herbs LLC is listed as the recalling firm, operating out of Cedar Rapids, IA. Federal records list the affected scope as 24 bottles.

The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: 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.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Dietary Supplements recalls over time

Where this recall sits in its category - 2,012 dietary supplements recalls on record

0100200300400 20072010201320162019202220252026 19
Severity1902064468High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

Iowa Select Herbs LLC, Burdock Root, www.iowaselectherbs.com, 4 fl. Oz.., Cedar Rapids, IA 52402

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.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Low (Class III)
Status Terminated
Recall number F-1154-2016
Date reported May 11, 2016
Date initiated September 11, 2015
Recalling firm Iowa Select Herbs LLC
Firm location Cedar Rapids, IA
Affected scope 24 bottles
Distribution 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.

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (F-1154-2016) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
Iowa Select Herbs LLC, Burdock Root, www.iowaselectherbs.com, 4 fl. Oz.., Cedar Rapids, IA 52402. Recalled by Iowa Select Herbs LLC. Units affected: 24 bottles.
Why was this product 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 agency issued this recall?
This recall was issued by the FDA Food on May 11, 2016. Severity: Low. Recall number: F-1154-2016.
Where was the recalled product distributed?
Distribution: 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 are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Compare this recall with Modern Warrior Ready, Dietary Supplement, 60 CAPSULES → · All Dietary Supplements recalls

This recall: FDA Food, reported May 11, 2016. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026