Severity
Low
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….
Sourced from official FDA Food enforcement records. Verify recall #F-1237-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1237-2016) 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 indicate 2 bottles units are affected.
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.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC and NHTSA going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 10 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified low severity.
Severity
Low
Units Affected
2 bottles
Related Recalls
6
0 from same agency
Iowa Select Herbs LLC, Yucca Root (Yucca aloifolia) www.iowaselectherbs.com, 1 Gallon., 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 supplements.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-1237-2016 |
| Date reported | May 11, 2016 |
| Date initiated | September 11, 2015 |
| Recalling firm | Iowa Select Herbs LLC |
| Units affected | 2 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.
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Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported May 11, 2016.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).