CLASS I Food recall · Reported 9 Aug 2017 · FDA Enforcement Report

Black Beans Bonanza Tamales with black beans recalled by Primavera Nueva

Primavera Nueva is recalling Black Beans Bonanza Tamales with black beans, distributed in California. The recall was initiated on 27 Jun 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNo lot codes: Expiry Date 7/3/17.
Quantity recalled240 packages (4 tamales per package)

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-2964-2017
FDA event ID
77779
Recalling firm
Primavera Nueva, Sonoma, CA
Classification
Class I
Status
Terminated
Recall initiated
27 Jun 2017
FDA classified
1 Aug 2017
Reported
9 Aug 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Beans & Lentils

Timeline

27 Jun 2017Recall initiated by company
1 Aug 2017Classified by FDA+35 days
9 Aug 2017Published 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

the product contains undeclared milk (in the cheese)

Product as listed by the FDA

Black Beans Bonanza Tamales with black beans. No Dairy:

Where it was distributed

CA only

California

Questions about this recall

Why was it recalled?

the product contains undeclared milk (in the cheese)

Which lots are affected?

No lot codes: Expiry Date 7/3/17.

Where was it sold?

CA only

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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