CLASS I Food recall · Reported 26 Sep 2012 · FDA Enforcement Report

"Tres Monjitas***Pineapple and guava beverage***Distribuido recalled

Vaqueria Tres Monjitas is recalling "Tres Monjitas***Pineapple and guava beverage***Distribuido por Vaquer¿a Tres Monjitas, distributed in Puerto Rico. The recall was initiated on 1 Aug 2012 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNo codes
Quantity recalled44,764 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-2360-2012
FDA event ID
62789
Recalling firm
Vaqueria Tres Monjitas, San Juan, PR
Classification
Class I
Status
Terminated
Recall initiated
1 Aug 2012
FDA classified
20 Sep 2012
Reported
26 Sep 2012
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Allergens
Product category
Mangoes

Timeline

1 Aug 2012Recall initiated by company
20 Sep 2012Classified by FDA+50 days
26 Sep 2012Published 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

Juice beverage contains undeclared allergenic sub-ingredient (sodium caseinate).

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

"Tres Monjitas***Pineapple and guava beverage***Distribuido por Vaquer¿a Tres Monjitas Inc***" Package sizes: gallons, 1/2 gallons, quarts, 14 oz and 8 oz.

Where it was distributed

PR only

Puerto Rico

Questions about this recall

Why was it recalled?

Juice beverage contains undeclared allergenic sub-ingredient (sodium caseinate).

Which lots are affected?

No codes

Where was it sold?

PR 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 21 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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