Pimento Cheese
Reason Pimento cheese was mislabeled with an ingredient list, which did not declare the presence of mayonnaise, containing egg sub-ingredient.
Tom Yom Soup recall
Recalled by Whole Foods Market Mid-Atlantic Kitchen · Landover, MD, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Ready to eat soup lists whey in the ingredient statement, but the product does not declare milk as the source for the allergen.
Undeclared allergen: Milk
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
Tom Yom Soup, 24 oz. plastic cups, packed 6 cups\cardboard case, and labeled in part ***Manufactured by Whole Foods Market, Landover, MD 20785***UPC 00000601467***
Quantity: 504 cups
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.
Use by 4/8/14
Where it was sold
Kentucky Maryland New Jersey Ohio Pennsylvania Virginia Washington
FDA's distribution note: Product was distributed to MD, NJ, OH, VA, KY, PA, and Washington, D.C.
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; 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 Mid-Atlantic Kitchen
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 19, 2014
- In FDA report of
- Apr 9, 2014
- Terminated
- Apr 8, 2014
- FDA recall number
- F-1743-2014 · event 67577
- Official record
- FDA enforcement report search