Iherb Solumeve Hydrolyzed Collagen Peptides Recall: Undeclared Milk Hazard
Iherb recalls Solumeve Hydrolyzed Collagen Peptides due to undeclared milk in MCT ingredient. Consumers should check UPC 8 98220 01828 4 for affected products.
Lower-risk recall
Informed by contract manufacturer that the MCT ingredient used in their product was under recall due to undeclared milk.
Contact the company
What happened, in plain English
Iherb is recalling Solumeve Hydrolyzed Collagen Peptides because the MCT ingredient contains undeclared milk. This could cause allergic reactions in people sensitive to milk. The recall affects products sold with the UPC 8 98220 01828 4. Read more at govinfonow.com/recall/14484-iherb-solumeve-hydrolyzed-collagen-peptides-recall-undeclared-milk-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/14484-iherb-solumeve-hydrolyzed-collagen-peptides-recall-undeclared-milk-hazard · Updated October 4, 2026 · FDA enforcement record: FDA #F-0846-2021
Cite this page
“Iherb Solumeve Hydrolyzed Collagen Peptides Recall: Undeclared Milk Hazard.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14484-iherb-solumeve-hydrolyzed-collagen-peptides-recall-undeclared-milk-hazard. Based on FDA recall #F-0846-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0846-2021%22&limit=1).
Why it’s dangerous
The MCT ingredient used in the product was recalled by its manufacturer for containing undeclared milk. This poses a risk for individuals with milk allergies who may react to the milk protein.
Who’s affected
People who own or use the Solumeve Hydrolyzed Collagen Peptides product with UPC 8 98220 01828 4 are affected. Those with milk allergies are at higher risk.
How to tell if you have this one
Check for the UPC code 8 98220 01828 4 on the product label. The product is a dietary supplement with net weight 14.1 oz (400g).
- Brand
Iherb- Product
Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supplement, NET Wt. 14.1 oz. (400g) Suggested- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 8 98220 01828 4 on the product label to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed in 30 states, and outside the U.S.
FDA distribution: “Direct sales to customers in AL, AZ, CA, CO, CT, DE, FL, GA, IL, KY, MA, MD, ME, MN, MO, MS,MT, NC, NJ, NM, NV, NY, OH, OR, PA, SC, TN, TX, VA, WA. Foreign customers in UA, UZ, VN, TR, TH, SI, SG, SE, SA, RO, QA, PT, PL, PH, PE, OM, NZ,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Illinois, Kentucky, Maine, Maryland, Massachusetts, Minnesota, Mississippi, Missouri, Montana, Nevada, New Jersey, New Mexico, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if I have the recalled product?
The recall does not include a specific remedy, so check the product label to confirm and contact Iherb for further instructions.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0846-2021 (May 24, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0846-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.