Pumpkin Spice No Bake Cookie
Reason Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product.
HomeFresh FOODS Suya Barbecue Seasoning recall
Recalled by Ellgof Inc. · Worcester, MA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product contains undeclared peanuts.
Undeclared allergen: Peanut
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
HomeFresh FOODS Suya Barbecue Seasoning, UPC: 6 033000120298, Net Wt: 240g/0.53 lbs; Produced in Ghana by: ELSSY KESS COMPANY LTD GHANA
Quantity: 144 jars
Food: Spices & seasonings
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.
MFG DATE: 31 AUG 2017 EXP DATE: 1 AUG 2020 BATCH No: EK 08 17
Where it was sold
Massachusetts New York
FDA's distribution note: MA and NY
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 peanut; 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
- Ellgof Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 4, 2018
- In FDA report of
- Feb 20, 2019
- Terminated
- Mar 15, 2019
- FDA recall number
- F-0872-2019 · event 81728
- Official record
- FDA enforcement report search
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