Buffalo Burgers ( 100% Pure Canadian Bison Meat ) recall
Recalled by Northfork Bison Distributions Inc. · Saint-Leonard, N/A, Canada
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Out of the abundance of caution, NORTHFORK BISON DISTRIBUTIONS INC. IS VOLUNTARILY RECALLING BISON BURGERS & GROUND BECAUSE OF POTENTIAL CONTAMINATION BY E. COLI: 0121 AND 0103.
Pathogen: E. coli
Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Buffalo Burgers ( 100% Pure Canadian Bison Meat ), Net Weight 16 oz. (1 lb ) 4 - 113 g Patties - individually frozen / per container / Box
Quantity: 1,904 BOXES; TOTAL WEIGHT 19,230 LBS
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.
N/A
Where it was sold
Arizona Florida Missouri New Jersey New York Pennsylvania Virginia Vermont
FDA's distribution note: GOODS WERE DISTRIBUTED ACROSS THE STATES OF NEW YORK, NEW JERSEY, PENNSYLVANIA, FLORIDA, MISSOURI, VERMONT, VIRGINIA AND ARIZONA TO DISTRIBUTION, INSTITUTIONS AND RETAIL OUTLETS.
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. 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
- Northfork Bison Distributions Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 12, 2019
- In FDA report of
- Aug 14, 2019
- Terminated
- Dec 11, 2020
- FDA recall number
- F-2080-2019 · event 83338
- Official record
- FDA enforcement report search