Griffith Labs Dry Milk and Egg Mix Recalled for Salmonella Risk
Griffith Labs U.S.A. is recalling Dry Milk and Egg Mix due to potential Salmonella contamination from a recalled whey ingredient.
The agency’s classification
FDA (Food): 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 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a high-risk pathogen (Salmonella) without reported illness, which corresponds to a High severity score per the rubric.
Plain-English summary
Griffith Labs U.S.A. is recalling 57 cases (1,026 lbs) of Dry Milk and Egg Mix, 12 oz bag, 24 bags per carton (Item 915004800). The recall is due to the potential presence of Salmonella caused by the use of a recalled whey ingredient.
The affected product, identified by batch or lot number 677185, was distributed nationwide and in Canada. The FDA has classified this recall as Class II.
Consumers who have purchased this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Dry Milk and Egg Mix 12 oz bag, 24 bags per carton Item 915004800
- Manufacturer
- Griffith Labs U.S.A.
- Category
- Food — Baking Mixes
- Hazard
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 (1)
- Batch or lot numbers: 677185
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 43 recalled by Griffith Labs U.S.A. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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