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CriticalFDAfda-F-0301-2020LISTERIA

Kale Cabbage Blend - Mann 4 x 2 lbs. UPC:10716519034623 - Food Service 6 x10 oz. UPC:68820133056 Canada COM

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
1,286,466
Recall Date
November 3, 2019
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0301-2020.

CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0301-2020.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Mann Packing Company, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0301-2020.

Mann Packing Company, Inc.

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Mann Packing Company, Inc. Recall FAQ

Mann Packing Company, Inc. is the subject of a food safety report: Kale Cabbage Blend - Mann 4 x 2 lbs. UPC:10716519034623 - Food Service 6 x10 oz. UPC:68820133056 Canada COM. The notice was published on November 3, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 1,286,466 units are potentially affected.