CLASS II Food recall · Reported 4 Apr 2018 · FDA Enforcement Report

Kids Bar Chocolate and Mixed Berry recalled by IDLife

IDLife is recalling Kids Bar Chocolate and Mixed Berry (. The recall was initiated on 5 Mar 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Numbers: A3617-1, 03047-1
Quantity recalled690

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
F-0977-2018
FDA event ID
79422
Recalling firm
IDLife, Frisco, TX
Brand
Kids
Classification
Class II
Status
Terminated
Recall initiated
5 Mar 2018
FDA classified
27 Mar 2018
Reported
4 Apr 2018
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Allergens
Product category
Granola Bars

Timeline

5 Mar 2018Recall initiated by company
27 Mar 2018Classified by FDA+22 days
4 Apr 2018Published 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

IDLife Kids Bar is labeled as nut free. Allergen testing indicated the presence of almonds and coconut.

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

IDLife Kids Bar Chocolate and Mixed Berry (SKU 16-0013) Organic, non-GMO, gluten-free and nut-free snack bar for children. Individually wrapped bars, packaged 10 to a box

Where it was distributed

United States

Questions about this recall

Why was it recalled?

IDLife Kids Bar is labeled as nut free. Allergen testing indicated the presence of almonds and coconut.

Which lots are affected?

Lot Numbers: A3617-1, 03047-1

Where was it sold?

United States

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.

Other products in this recall event

2 other products · FDA event 79422

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