Kindroot Peach Blossom Plant Lozenges Recall: Missing Fish Collagen Source
Kindroot recalls Peach Blossom Plant lozenges for dietary supplements due to missing fish as collagen source. Label error may mislead consumers about collagen content.
Lower-risk recall
Inspection by California Department of Public Health found that product label did not include fish as the source of collagen peptides.
Contact the company
What happened, in plain English
Kindroot is recalling Peach Blossom Plant lozenges because the product label does not list fish as the source of collagen peptides. This could mislead consumers about the product's actual collagen content. Read more at govinfonow.com/recall/15992-kindroot-peach-blossom-plant-lozenges-recall-missing-fish-collagen-source.
Source Summary by GovInfoNow · govinfonow.com/recall/15992-kindroot-peach-blossom-plant-lozenges-recall-missing-fish-collagen-source · Updated October 5, 2026 · FDA enforcement record: FDA #F-0573-2020
Cite this page
“Kindroot Peach Blossom Plant Lozenges Recall: Missing Fish Collagen Source.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15992-kindroot-peach-blossom-plant-lozenges-recall-missing-fish-collagen-source. Based on FDA recall #F-0573-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0573-2020%22&limit=1).
Why it’s dangerous
The product label incorrectly states the collagen source without mentioning fish. This could mislead consumers into thinking the product contains collagen from fish when it does not, potentially affecting their dietary supplement choices.
Who’s affected
People who purchased Kindroot Peach Blossom Plant lozenges for dietary supplements are affected. Those most at risk are consumers who rely on the product for collagen intake.
How to tell if you have this one
Check for Kindroot Peach Blossom Plant lozenges with 20 tablets, 2.6 oz (74 g) net weight. Look for lot numbers 1109192, 1117192, 1124192, or 1221192 on the label.
- Brand
Kindroot- Product
kindroot adaptogems; Peach Blossom Plant lozenges for lit looks. 20 lozenges net wt. 2.6 oz. 74 g - Dietary Supplement- Category
Food
What to do — step by step
Check Product Label
Look for the lot numbers 1109192, 1117192, 1124192, or 1221192 on the label to identify affected items.
Where it went and when
Where it was distributed
Distributed in 6 states.
FDA distribution: “CA NY, VA and 18 online sales on to customers in CA, OH, AK, CO.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alaska, California, Colorado, New York, Ohio, Virginia.
Recall timeline
FDA terminated this recall 40 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- 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
Is there a risk of serious injury from this product?
No, the recall is for labeling accuracy, not a safety hazard.
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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-0573-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0573-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.