CLASS I Food recall · Reported 25 Dec 2013 · FDA Enforcement Report
Tres Leches, Lymar, Peso Neto, Ponce, Puerto Rico recalled
Flanes Lymar is recalling Tres Leches, Lymar, Peso Neto, Ponce, Puerto Rico, distributed in Puerto Rico. The recall was initiated on 29 Oct 2013 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-0828-2014
- FDA event ID
- 66676
- Recalling firm
- Flanes Lymar, Ponce, PR
- Brand
- Tres Leches
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 29 Oct 2013
- FDA classified
- 13 Dec 2013
- Reported
- 25 Dec 2013
- 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
- Other
Timeline
| 29 Oct 2013 | Recall initiated by company | |
| 13 Dec 2013 | Classified by FDA | +45 days |
| 25 Dec 2013 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared allergens: eggs, wheat and soy
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 Leches, Lymar, Peso Neto 3 oz, Ponce, Puerto Rico
Where it was distributed
Puerto Rico only.
Questions about this recall
Why was it recalled?
Undeclared allergens: eggs, wheat and soy
Which lots are affected?
none
Where was it sold?
Puerto Rico 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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