CLASS I Food recall · Reported 17 Jun 2015 · FDA Enforcement Report
Cheese / Guava Cake recalled by AYAA Popcorn Manufacturing
AYAA Popcorn Manufacturing is recalling Cheese / Guava Cake. The recall was initiated on 17 Oct 2014 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-2435-2015
- FDA event ID
- 69447
- Recalling firm
- AYAA Popcorn Manufacturing, San Juan, PR
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 17 Oct 2014
- FDA classified
- 11 Jun 2015
- Reported
- 17 Jun 2015
- 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
- Cakes & Pastries
Timeline
| 17 Oct 2014 | Recall initiated by company | |
| 11 Jun 2015 | Classified by FDA | +237 days |
| 17 Jun 2015 | 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
FDA inspection disclosed product labels with undeclared milk.
Product as listed by the FDA
Cheese / Guava Cake 2 oz
Where it was distributed
Product distributed to local Supermax Supermarket Stores
Questions about this recall
Is Cheese / Guava Cake recalled?
Yes. AYAA Popcorn Manufacturing recalled Cheese / Guava Cake on 17 Oct 2014. The recall is Class I and its status is Terminated. Recall number F-2435-2015.
Why was it recalled?
FDA inspection disclosed product labels with undeclared milk.
Which lots are affected?
Expiration Date: 8/8/2014 to 11/19/2014
Where was it sold?
Product distributed to local Supermax Supermarket Stores
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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