GRANDMA'S perogies POTATO & BACON PEROGIES recall
Recalled by Buffalo Sav, INC. · Buffalo, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Buffalo SAV, Inc. has recalled GRANDMA'S perogies POTATO & BACON PEROGIES due to the presence of Undeclared Soy.
Undeclared allergen: Soy
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
GRANDMA'S perogies POTATO & BACON PEROGIES, NET WEIGHT 907 g (32 oz/2 lb), UPC 8 92691 00112 7. Product packed in plastic bag with pink label and contains 14 - 2 lb bags per case. Manufactured by S&A Grandma's Food Inc. 196-44 Fasken Drive Toronto, ON M9W 5M8 (416) 679-8444, www.grandmafoods.com. Product of Canada.
Quantity: 128 cases (14 - 2 lb bags per case)
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.
expiration date 040414 to 040415
Where it was sold
California Illinois Indiana Michigan New York Ohio
FDA's distribution note: CA, IN, NY, OH, MI, and IL
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 soy; 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
- Buffalo Sav, INC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 8, 2014
- In FDA report of
- Nov 12, 2014
- Terminated
- Mar 28, 2017
- FDA recall number
- F-0095-2015 · event 67945
- Official record
- FDA enforcement report search