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CriticalFDAfda-F-1836-2016LISTERIA

Sunflower Seeds, PLU# 65167; various weights; various sell by dates; Market District; Distributed by Giant Eagle, Pittsburgh, PA 15238

⚠ 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
2,197
Recall Date
May 3, 2016
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1836-2016.

Giant Eagle supplier SunOpta has informed Giant Eagle of the expansion of their sunflower kernel recall due to possible Listeria monocytogenes contamination. Giant Eagle repacked the sunflower kernels under the Market District label, which were sold in the bulk section of 12 of its Market District stores. Giant Eagle has expanded their recall to include all lots of sunflower seeds

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1836-2016.

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 Giant Eagle, 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-1836-2016.

Giant Eagle, Inc.

FDA

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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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Giant Eagle, Inc. Recall FAQ

Giant Eagle, Inc. is the subject of a food safety report: Sunflower Seeds, PLU# 65167; various weights; various sell by dates; Market District; Distributed by Giant Eagle, Pittsburgh, PA 15238. The notice was published on May 3, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 2,197 units are potentially affected.