CLASS II ONGOING Food recall · Reported 11 Jun 2025 · FDA Enforcement Report

Eudos Bronquilan recalled by Nature's Eudos Distributors

Nature's Eudos Distributors is recalling Eudos Bronquilan, distributed in New Jersey, New York. The recall was initiated on 1 Jun 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codeslot #084216, Ex. Date 9/6/2027
Quantity recalled700 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0007-2025
FDA event ID
96963
Recalling firm
Nature's Eudos Distributors, Milford, CT
Classification
Class II
Status
Ongoing
Recall initiated
1 Jun 2025
FDA classified
3 Jun 2025
Reported
11 Jun 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Other

Timeline

1 Jun 2025Recall initiated by company
3 Jun 2025Classified by FDA+2 days
11 Jun 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared colors (FD&C Yellow #5, FD&C Blue #1, and FD&C Red #40)

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Eudos Bronquilan

Where it was distributed

NY, NJ

New JerseyNew York

Questions about this recall

Why was it recalled?

Undeclared colors (FD&C Yellow #5, FD&C Blue #1, and FD&C Red #40)

Which lots are affected?

lot #084216, Ex. Date 9/6/2027

Where was it sold?

NY, NJ

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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