Mini Cuban loaf cake with raisins recalled over undeclared FD&C Yellow 5
Catao Market is recalling 260 master cases (3,120 loaf cakes) of Mini Gaceniga Authentic Cuban Loaf Cake Raisins because the colour FD&C Yellow #5 was not declared on the label.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: Scored 2 under the minor labeling criterion: the record cites an undeclared colour additive with no stated illness or consequence.
Plain-English summary
Mini Gaceniga Authentic Cuban Loaf Cake Raisins, net weight 12 oz (340g), packaged in wax paper placed in a clear bag and packed in a cardboard carton, 12 x 12 oz per master case, is being recalled by Catao Market LLC.
The reason given in the enforcement record is undeclared colors, FD&C Yellow #5.
The record lists 260 master cases (3,120 loaf cakes), identified by best-by dates from 12/18/2025 through 03/18/2026. The product was distributed only in Florida. The FDA has classified the action as Class II.
The record cites an undeclared colour additive rather than a pathogen or major allergen, and reports no illnesses. Consumers should follow the retailer's return instructions.
The recalled product
- Product
- ICU Medical Plum Duo Precision IV Pump, List Numbers: 400020403 (US), 400021003 (Philippines)
- Manufacturer
- ICU Medical, Inc.
- Category
- Food — Bakery
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- 400020403 (US)
- Software Versions: 1.2.2
- 400021003 (Philippines)
- Software Versions: 1.2.0
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 recalled by ICU Medical, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 3 products in this recall →Related recalls
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