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CriticalFDAfda-F-0726-2016UNDECLARED ALLERGEN

Refrigerated, fresh, Panko breaded cod fillet packed in blue foam tray with plastic overwrap. Label reading: Giant Eagle Japanese Breade...

⚠ 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.

Units Affected
420
Recall Date
February 4, 2016
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0726-2016.

All lot codes up to and including February 8, 2016 of Giant Eagle brand Japanese Breaded Cod Fillets, prepared and sold from the Seafood department inside Giant Eagle and Market District supermarkets through February 4, 2016 have been voluntarily recalled by Giant Eagle due to an undeclared soy allergen.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0726-2016.

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-0726-2016.

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 bakery & grains safety report: Refrigerated, fresh, Panko breaded cod fillet packed in blue foam tray with plastic overwrap. Label reading: Giant Eagle Japanese Breade.... The notice was published on February 4, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 420 units are potentially affected.