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Food Recall Radar
Class IUSDA FSIS008

Jowett Farms Corporation Recalls Pork Products Produced without Benefit of Import Inspection

Class IA reasonable probability that eating this product will cause serious health problems or death.

Product

•20-oz. plastic wrapped tray packages containing sausage links of “Jewel-Osco Sheboygan Brand Bratwurst – Made in Illinois”; •20-oz. plastic wrapped tray packages containing sausage links of “Jewel-Osco Mild Italian Sausage”; •20-oz. plastic wrapped tray packages containing sausage links of “Jewel-Osco Hot Italian Sausage”

  • •20-oz. plastic wrapped tray packages containing sausage links of “Jewel-Osco Sheboygan Brand Bratwurst – Made in Illinois”
  • •20-oz. plastic wrapped tray packages containing sausage links of “Jewel-Osco Mild Italian Sausage”
  • •20-oz. plastic wrapped tray packages containing sausage links of “Jewel-Osco Hot Italian Sausage”

Reason for recall

Produced Without Benefit of Inspection

Agency notice

WASHINGTON, April 10, 2020 – Jowett Farms Corporation, a Blumenort, Canada establishment, is recalling approximately 42,587 pounds of raw pork trimmings that were not presented for import re-inspection into the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The raw pork trimmings were imported on April 2, 2020 and further processed into sausage products. The following products are subject to recall: [View Labels (PDF Only)]

  • 20-oz. plastic wrapped tray packages containing sausage links of “Jewel-Osco Sheboygan Brand Bratwurst – Made in Illinois” with a sell-by date of 4/17/20.
  • 20-oz. plastic wrapped tray packages containing sausage links of “Jewel-Osco Mild Italian Sausage” with a sell-by date of 4/17/20.
  • 20-oz. plastic wrapped tray packages containing sausage links of “Jewel-Osco Hot Italian Sausage” with a sell-by date of 4/17/20.

The products subject to recall bear establishment number “EST. 7779” inside the USDA mark of inspection. These items were shipped to retail locations in Illinois and Wisconsin.                           

The problem was discovered during routine FSIS surveillance activities of imported products.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider. 

FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away.

FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website.

Related recalls

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