Recall record at a glance
| Official record | F-0726-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Giant Eagle, Inc. |
| Report date | Mar 16, 2016 |
| Recall initiation date | Feb 4, 2016 |
| Quantity | 420 units |
| Location | Pittsburgh, PA, United States |
Official product description
Refrigerated, fresh, Panko breaded cod fillet packed in blue foam tray with plastic overwrap. Label reading: Giant Eagle Japanese Breaded Cod Fillet various weights. Distributed by: Giant Eagle, Inc., Pittsburgh, PA 15238 Sold from August 2015 to present with various expiration dates.
Why the product was recalled
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.
Distribution information
PA OH
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.