Pharmanex Kids Jungamals Dietary Supplement: Missing Fish Allergen Label
Pharmanex recalls Kids Jungamals chewable tablets due to missing fish allergen statement on label, which could pose allergy risk for those with fish allergies.
Lower-risk recall
Pharmanex Jungamals was found to have a missing fish allergen statement on the label due to fish gelatin as a sub-component of the Vitamin E ingredient.
Contact the company
What happened, in plain English
Pharmanex is recalling Kids Jungamals dietary supplements because they lack a fish allergen statement on the label. This could be dangerous for people with fish allergies who might consume the product without knowing. Read more at govinfonow.com/recall/14090-pharmanex-kids-jungamals-dietary-supplement-missing-fish-allergen-label.
Source Summary by GovInfoNow · govinfonow.com/recall/14090-pharmanex-kids-jungamals-dietary-supplement-missing-fish-allergen-label · Updated October 4, 2026 · FDA enforcement record: FDA #F-0095-2022
Cite this page
“Pharmanex Kids Jungamals Dietary Supplement: Missing Fish Allergen Label.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14090-pharmanex-kids-jungamals-dietary-supplement-missing-fish-allergen-label. Based on FDA recall #F-0095-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0095-2022%22&limit=1).
Why it’s dangerous
The supplement contains fish gelatin as a component of Vitamin E, but the label does not list fish as an allergen. This means people with fish allergies might not know they could be exposed to the allergen.
Who’s affected
Parents of children who use Pharmanex Kids Jungamals supplements are most at risk. Anyone with fish allergies should avoid this product due to the missing allergen label.
How to tell if you have this one
Check for the white bottle labeled 'Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tablets'. The batch code is CS11711 and expiration date is April 30, 2022.
- Brand
Pharmanex- Category
Food
What to do — step by step
Check Label
Look for the fish allergen statement on the label; if missing, stop using the product.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Distributed directly to consumers nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 6 months 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.
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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-0095-2022 (October 1, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0095-2022 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.