Kabobs Mini Classic French Quiche Recalled for E. coli O121 Contamination
Kabobs Inc is recalling Mini Classic French Quiche because it was 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. Per the rubric, FDA Class II recalls involving high-risk pathogens or significant injury/property-damage reports are classified as Severe (Score 4).
Plain-English summary
Kabobs Inc is voluntarily recalling 84 cases of Mini Classic French Quiche, 200 CT. The product was prepared by Kabobs, located at 54234 North Lake Dr., Lake City, GA 30260. The recall is due to the use of flour that was previously recalled for E. coli O121 contamination.
The affected product is identified by Item number K462 and Lot/Julian Code PM15M10 / 15344. 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.
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 has classified this recall as Class II, indicating 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
- MINI CLASSIC FRENCH QUICHE, 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: K462
- Lot/Julian Code: PM15M10 / 15344.
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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