Recall record at a glance
| Official record | F-1406-2020 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Giant Eagle |
| Report date | Sep 9, 2020 |
| Recall initiation date | Aug 2, 2020 |
| Quantity | Unknown |
| Location | Pittsburgh, PA, United States |
Official product description
STUFFED TURKEY BREAST GOURMET (INDEPENDENT PLU). PLU# 25093400000. Expiration date 8/5/2020. Ingredients: STUFFED TURKEY BREAST [TURKEY [TURKEY BREAST ROAST W 25% SOLUTION OF TURKEY BROTH, TURKEY SEASONING (MALTODEXTRIN, SALT, SUGAR, YEAST EXTRACT, DEXTROSE, TURKEY BROTH, ONION POWDER, GARLIC POWDER, NATURAL FLAVORS, POLYSORBATE 80), SODIUM PHOSPHATE, SALT], STUFFING [SPREAD (PURIFIED WATER, SOYBEAN OIL, PALM KERNEL & PALM OIL, SALT, SOY LECITHIN, VINEGAR, NATURAL FLAVORS, VITAMIN A PALMITATE, BETA CAROTENE [COLOR], VITAMIN D3), CROUTONS (ENRICHED BLEACHED WHEAT FLOUR [MALTED BARLEY FLOUR, NIACIN, IRON, POTASSIUM BROMATE, THIAMINE MONONITRATE, RIBOFLAVIN, FOLIC ACID], WATER, YEAST, SALT, DEXTROSE, SOYBEAN OIL, DATEM, CORNSTARCH, L-CYSTEINE, ASCORBIC ACID, AZODICARBONAMIDE, ENZYMES, CALCIUM PROPIONATE ADDED TO HELP RETARD SPOILAGE), CELERY, ONIONS, SALT, BLACK PEPPER], OIL BLEND [CANOLA OIL, EXTRA VIRGIN OLIVE OIL], SEASONING [SUGAR, SALT, CORN STARCH, PAPRIKA, SPICES, CONTAINS 2% OR LESS OF THE FOLLOWING: SOYBEAN OIL, OLEORESIN PAPRIKA, OIL OF LEMON, OIL OF ORANGE, CARAMEL COLOR], SALT].Onions are cooked.
Why the product was recalled
Potential contamination with Salmonella Newport in onions and prepared foods containing onions.
Distribution information
Product was produced and sold in Giant Eagle and Market District locations in IN, OH, MD, WV and PA.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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
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