Suspiros Chocoflan Cake.15 P: 13.7 servings (1712 gr). UPC=177. Type of packaging: Plastic dome and plate. Firm name: N
Summary
The FDA issued a Class III for Suspiros Chocoflan Cake.15 P: 13.7 servings (1712 gr). UPC=177. Type of packagi by NOVACAB SAPI DE CV. Reason: Multiple cake products contain goat milk, which was labeled as "milk".
Details
Source
Food Recall
External ID
H-0343-2025
Action Date
2025-08-06
Status
Terminated
Category
food
Product Description
Suspiros Chocoflan Cake.15 P: 13.7 servings (1712 gr). UPC=177. Type of packaging: Plastic dome and plate. Firm name: NOVACAB SAPI de CV. Address listed on label: El paso, TX 79901, USA.
Lot/Code Info: 06215 06235
Quantity Affected: 82 units
Reason for Recall
Multiple cake products contain goat milk, which was labeled as "milk"
Distribution
Distributed to three states: California, Arizona, and Texas
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-27
Company
Heroica Nogales
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
NOVACAB SAPI DE CV has 9 FDA actions in our database, including 9 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (NOVACAB SAPI DE CV) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does NOVACAB SAPI DE CV have FDA actions?
NOVACAB SAPI DE CV has 9 FDA actions in our database, including 9 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0343-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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