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CriticalFDAfda-F-1698-2016UNDECLARED ALLERGEN

The sunflower kernels roasted ( no salt) were packed in a 30 lbs. corrugated box with a poly liner with the following labeling: 1. ...

⚠ Critical Alert — Stop Using Immediately

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

Category
Units Affected
823
Recall Date
May 20, 2016
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1698-2016.

Firm recalling under directions from their Supplier, due to possible risk of product containing Listera monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1698-2016.

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 C.j. Dannemiller 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-1698-2016.

C.J. Dannemiller Company, Inc.

FDA

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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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C.j. Dannemiller Company, Inc. Recall FAQ

C.j. Dannemiller Company, Inc. is the subject of a food safety report: The sunflower kernels roasted ( no salt) were packed in a 30 lbs. corrugated box with a poly liner with the following labeling: 1. .... The notice was published on May 20, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 823 units are potentially affected.