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