CLASS I Food recall · Reported 11 Nov 2015 · FDA Enforcement Report

Cocoa buttons recalled by Biscomerica

Biscomerica is recalling Cocoa buttons, distributed in Ohio. The recall was initiated on 27 Oct 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLOT No. B073016, A092916, A021717, A021817, A030717, B030717, A031517, A031617, A033017, B033017
Quantity recalled3,595 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
F-0137-2016
FDA event ID
72510
Recalling firm
Biscomerica, Rialto, CA
Brand
Cocoa
Classification
Class I
Status
Terminated
Recall initiated
27 Oct 2015
FDA classified
5 Nov 2015
Reported
11 Nov 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Milk
Product category
Chocolate

Timeline

27 Oct 2015Recall initiated by company
5 Nov 2015Classified by FDA+9 days
11 Nov 2015Published in enforcement report+6 days

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

Reason for recall

Biscomerica is recalling cocoa buttons because it contains undeclared milk.

Product as listed by the FDA

Cocoa buttons, item no. 80203, 80203-1, 25lb bulk case

Where it was distributed

Ohio

Ohio

Questions about this recall

Why was it recalled?

Biscomerica is recalling cocoa buttons because it contains undeclared milk.

Which lots are affected?

LOT No. B073016, A092916, A021717, A021817, A030717, B030717, A031517, A031617, A033017, B033017

Where was it sold?

Ohio

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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