Publix Rice & Pigeon Peas
Reason Undeclared Allergen (Soy)
Taste of Inspirations Classic Red Skin Potato Salad recall
Recalled by ASK Foods Inc · Palmyra, PA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
A.S.K. Foods, Inc. of Palmyra, Pennsylvania is voluntarily recalling one lot of Taste of Inspirations Classic Red Skin Potato Salad because it may contain undeclared egg.
Undeclared allergen: Egg
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Taste of Inspirations Classic Red Skin Potato Salad; Creamy redskin potatoes & white onion in a tangy dressing. Net Wt. 16 OZ. Sell By: 08-01-16 4238
Quantity: N/A
Food: Onions Sauces, dips & dressings Salads, sandwiches & prepared foods
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Sell By: 08-01-16 4238
Where it was sold
Maine New Hampshire Vermont
FDA's distribution note: ME, NH, VT
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- ASK Foods Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 29, 2016
- In FDA report of
- Dec 14, 2016
- Terminated
- Jan 23, 2017
- FDA recall number
- F-0607-2017 · event 74858
- Official record
- FDA enforcement report search
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