Kabobs Four Cheese Puff Recalled Due to E. coli O121 Contamination
Kabobs Inc is recalling Four Cheese Puff products because they were manufactured with flour contaminated with E. coli O121.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall involves E. coli O121, a high-risk pathogen, and is classified as FDA Class II. Per the rubric, FDA Class II recalls involving significant pathogens or injury risks are rated as Severe (4).
Plain-English summary
Kabobs Inc is recalling 28 cases of Four Cheese Puff (200 units per case) because the product was manufactured with flour that was recalled due to E. coli O121 contamination. The affected product is identified by Item number K7234 and Lot/Julian Code PM16A13 / 16013.
The recall covers distribution in the following states: AR, CA, CO, CT, FL, GA, IL, IN, IO, KY, LA, MA, MD, MI, MN, MO, NC, NJ, NY, NV, OK, OH, OR, PA, TN, TX, WA, and WI. The product was prepared by Kabobs, located at 54234 North Lake Dr., Lake City, GA 30260.
Consumers should check their pantries for this specific product and lot code. If found, they should discard the product or return it to the place of purchase. The FDA classifies this as a Class II recall, indicating a situation in which there is a reasonable probability that the use of or exposure to the violative product may cause temporary or medically reversible adverse health consequences.
The recalled product
- Product
- FOUR CHEESE PUFF, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260
- Manufacturer
- Kabobs Inc
- Category
- Food — Bakery / Prepared Foods
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 (2)
- Item number: K7234
- Lot/Julian Code: PM16A13 / 16013.
Distribution
Part of a larger recall action
This product is one of 27 recalled by Kabobs Inc 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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