CLASS I Food recall · Reported 29 Aug 2018 · USDA FSIS
Beef and Pork Meatloaf Products recalled by Taylor Farms Illinois
Taylor Farms Illinois is recalling Array. The recall was initiated on 29 Aug 2018 and the FDA has classified it as Class I.
Recall details
- Recall number
- FSIS-070-2018
- Recalling firm
- Taylor Farms Illinois
- Classification
- Class I
- Status
- Completed
- Recall initiated
- 29 Aug 2018
- Reported
- 29 Aug 2018
- USDA notice type
- Closed Recall
- Reason category
- Undeclared Egg
- Product category
- Beef
Timeline
| 29 Aug 2018 | Recall initiated by company | |
| 29 Aug 2018 | Published in enforcement report | +0 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Array. WASHINGTON, Aug. 29, 2018 Taylor Farms Illinois, Inc., a Chicago, Ill. establishment, is recalling approximately 75 pounds of beef and pork meatloaf products due to misbranding and undeclared allergens, the U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) announced today. The product contains eggs and wheat, known allergens, which are not declared on the product label. The beef and pork meatloaf was produced on August 22, 2018. The following products are subject to recall: [View Labels (PDF only)] 14-oz. plastic tray packages containing ready-to-eat HOMESTYLE BEEF AND PORK MEATLOAF with lot code TFIL234A001 and a USE-BY: 08/28/18 date on the label. The products subject to recall bear establishment number EST. 21794 inside the USDA mark of inspection. These items were shipped to retail locations in Alabama, Arkansas, Kentucky, Mississippi, Ohio and Tennessee. The problem was discovered on August 27, 2018, by a retail store employee, who then reported the issue to the firm. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. FSIS is concerned that some product may be frozen and in consumers freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify that recal
Product as listed by the USDA
Array
Where it was distributed
Array
Questions about this recall
Why was it recalled?
Array. WASHINGTON, Aug. 29, 2018 Taylor Farms Illinois, Inc., a Chicago, Ill. establishment, is recalling approximately 75 pounds of beef and pork meatloaf products due to misbranding and undeclared allergens, the U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) announced today. The product contains eggs and wheat, known allergens, which are not declared on the product label. The beef and pork meatloaf was produced on August 22, 2018. The following products are subject to recall: [View Labels (PDF only)] 14-oz. plastic tray packages containing ready-to-eat HOMESTYLE BEEF AND PORK MEATLOAF with lot code TFIL234A001 and a USE-BY: 08/28/18 date on the label. The products subject to recall bear establishment number EST. 21794 inside the USDA mark of inspection. These items were shipped to retail locations in Alabama, Arkansas, Kentucky, Mississippi, Ohio and Tennessee. The problem was discovered on August 27, 2018, by a retail store employee, who then reported the issue to the firm. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. FSIS is concerned that some product may be frozen and in consumers freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify that recal
Where was it sold?
Array
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official USDA FSIS notice · Source record retrieved 29 Sep 2026. USDA data is public domain. This page reports the record and gives no medical advice.
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