Maine Grains Inc recall
Recalled by Maine Grains, Inc · Skowhegan, ME, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product contains 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
Maine Grains Inc. brand Organic Yellow Peas sold between 10/17/2019 and 11/1/2020; product was packaged in 25lb bulk bags, 12 x 1lb cases; and clear cellophane 1lb bags sold online and labelled as "Crop Rotation Organic Yellow Peas"
Quantity: 2,000lbs
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.
Sold between 10/17/2019 and 11/1/2020.
Where it was sold
California Colorado Connecticut Florida Georgia Iowa Massachusetts Maine North Carolina New Hampshire New Jersey New York Ohio Pennsylvania Rhode Island Virginia Vermont
FDA's distribution note: ME, MA, VT, NY, NH, CT, GA, RI, PA, NJ, OH, VA, FL, NJ, NC, CA, IA, CO
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
- Maine Grains, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 26, 2021
- In FDA report of
- Feb 17, 2021
- Terminated
- Jul 23, 2021
- FDA recall number
- F-0275-2021 · event 87225
- Official record
- FDA enforcement report search