Cahill Whiskey Cheddar Cheese packaged in clear plastic PLU 5478494884
Reason Potential to be contaminated with Listeria monocytogenes
Chantilly Key Lime Tartlets recall
Recalled by Whole Foods Market · Austin, TX, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential to contain undeclared tree nuts (almond)
Undeclared allergen: Tree nuts
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
Chantilly Key Lime Tartlets Net Wt 1 oz. individually packaged in plastic clamshell containers with Whole Foods Market scale labels, a PLU code of 268564
Quantity: 165 Units
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.
PLU code of 2685640000, and product sell-by date through July 26, 2020
Where it was sold
Connecticut Massachusetts Maine New Hampshire Rhode Island
FDA's distribution note: Connecticut, Maine, Massachusetts, New Hampshire and Rhode Island
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 tree nuts; 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
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 23, 2020
- In FDA report of
- Aug 12, 2020
- Terminated
- Nov 3, 2020
- FDA recall number
- F-1048-2020 · event 86117
- Official record
- FDA enforcement report search
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