Iowa Select Herbs LLC, Goldenseal Root (Hydrastis canadensis), www.iowaselectherbs.com…
Iowa Select Herbs LLC recalled this product and the FDA reported the enforcement action on 11 May 2016 as Class III. The recall was mandated. 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.

The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Iowa Select Herbs LLC, Goldenseal Root (Hydrastis canadensis), www.iowaselectherbs.com, (a) 4 fl. Oz. (b) 32 fl. Oz. (c) 1 gallon, 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.
- Recalling firm
- Iowa Select Herbs LLC
- Firm location
- Cedar Rapids, Iowa, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- F-1179-2016
- Quantity
- (a) 1 bottle, (b) 1 bottle, (c) 1 bottle
- 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.
- Initiated
- 11 September 2015
- Reported by FDA
- 11 May 2016
- Terminated
- 27 February 2017
- Firm notified by
- Press Release
- Product codes
- Lot - 32996, Expires - 09/2019;
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- This recall was not recorded as firm-initiated. The circumstances in which the FDA requests a recall are set out in 21 CFR 7.45.
- This is one of 104 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 104 separate recalls, which almost every published figure does, overstates it by a factor of 104. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 104 of them.
- The recall ran for 18 months, from 11 September 2015 to termination on 27 February 2017. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 8 states, and the FDA published the enforcement report 8 months after the firm began the recall.
- Recalls of fresh produce run a median of 7 months, so this one was longer than usual for its category. Fresh produce is the category where contamination arrives before the facility does: irrigation water, soil amendments and field workers are the routes, and nothing downstream of the farm is a kill step for a product eaten raw.
Named in the distribution pattern: Florida, Georgia, Iowa, Michigan, Missouri, Montana, New York, South Carolina. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Unapproved ingredients
An unapproved ingredient recall means a product contained a substance not permitted in food, most often an undisclosed pharmaceutical active found in a dietary supplement.
A preventive controls plan covers an unapproved ingredient under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 111
- Dietary supplement CGMP: the identity, purity, strength and composition specifications a supplement manufacturer sets and verifies for every component and finished batch.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
Filed under fresh produce. A product can sit in more than one.
Other fresh produce recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Iowa Select Herbs LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 103 other records name this firm.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2016-05-11 | Iowa Select Herbs LLC, Burdock Root, www.iowaselectherbs.com, 4 fl. Oz.., Cedar Rapids, IA 52402 | Iowa Select Herbs LLC | 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. | Class III |
| 2016-05-11 | Iowa Select Herbs LLC, Acerola Berry (Malpighia), www.iowaselectherbs.com, 4 fl. Oz. (120 ml), Cedar Rapids, IA 52402 | Iowa Select Herbs LLC | 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. | Class III |
| 2016-05-11 | Iowa Select Herbs LLC, Damiana Leaf (Turnera diffusa), www.iowaselectherbs.com, 1 gallon, Cedar Rapids, IA 52402 | Iowa Select Herbs LLC | 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. | Class III |
| 2016-05-11 | Iowa Select Herbs LLC, Lemon Balm Leaf (Melissa officinalis), www.iowaselectherbs.com, (a) 1 fl. Oz., (b) 4 fl. Oz., (c) 8 fl. Oz., (d) 16 fl. Oz., (e) 32 fl. Oz., Cedar Rapids, IA 52402 | Iowa Select Herbs LLC | 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. | Class III |
| 2016-05-11 | Iowa Select Herbs LLC, Reishi Mushroom (Ganoderma Lucidum), www.iowaselectherbs.com, 7.5 fl. Oz., Cedar Rapids, IA 52402 | Iowa Select Herbs LLC | 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. | Class III |
| 2016-05-11 | Iowa Select Herbs LLC, Kava Kava Root (Piper methysticum), www.iowaselectherbs.com, (a) 2 fl. Oz., (b) 4 fl. Oz., (c) 16 fl. Oz., Cedar Rapids, IA 52402 | Iowa Select Herbs LLC | 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. | Class III |
| 2016-05-11 | Iowa Select Herbs LLC, Red Ginseng Root (Panax ginseng), www.iowaselectherbs.com, 7.5 fl. Oz., Cedar Rapids, IA 52402 | Iowa Select Herbs LLC | 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. | Class III |
| 2016-05-11 | Iowa Select Herbs LLC, Olive Leaf (Olea europa), www.iowaselectherbs.com, (a) 4 fl. Oz. (b) 16 fl. Oz., (c) 1 gallon (d) Unknown size. Cedar Rapids, IA 52402 | Iowa Select Herbs LLC | 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. | Class III |
| 2016-05-11 | Iowa Select Herbs LLC, Licorice Root (Glycyrrhiza glabra), www.iowaselectherbs.com, (a) 2 fl. Oz., (b) 4 fl. Oz., (c) 16 fl. Oz., Cedar Rapids, IA 52402 | Iowa Select Herbs LLC | 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. | Class III |
| 2016-05-11 | Iowa Select Herbs LLC, Milk Thistle Seed (Carduus marianus), www.iowaselectherbs.com, (a) 4 fl. Oz., (b) 16 fl. Oz., (c) 32 fl. Oz., Cedar Rapids, IA 52402 | Iowa Select Herbs LLC | 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. | Class III |
All 104 records for Iowa Select Herbs LLC
All 2016 recalls · All FDA food recall data
21 CFR 111 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.