Whole Foods Market Everyday Double Crust Apple Pie sold in clear…
Reason Whole and sliced Apple and Cherry Pies from five stores in the Mid-Atlantic Region contain undeclared milk and egg.
Whole Foods Market Everyday Double Crust Cherry Pie sold in clear… recall
Recalled by Whole Foods Market Brand 365, Llc · Austin, TX, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Whole and sliced Apple and Cherry Pies from five stores in the Mid-Atlantic Region contain undeclared milk and egg.
Undeclared allergens: Milk 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
Whole Foods Market Everyday Double Crust Cherry Pie sold in clear plastic clamshell with scale label applied. Sold as whole pie or by the slice. PLUs 74874, 74401, 33405
Quantity: 548 pies (total)
Food: Bread & bakery
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 Dates : 9/202021-9/27/2021
Where it was sold
Maryland Pennsylvania Virginia
FDA's distribution note: MD, PA, VA
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 milk, 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
- Whole Foods Market Brand 365, Llc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 22, 2021
- In FDA report of
- Oct 27, 2021
- Terminated
- Dec 8, 2021
- FDA recall number
- F-0025-2022 · event 88765
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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