Food Recall Check
Class III · Low risk Terminated Initiated Jan 6, 2020 (7 years ago)

Dry Garbanzo Beans are sold under different brands and described as follows recall

Recalled by Columbia Bean & Produce, Inc. · Moses Lake, WA, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

11.8 ppm of glyphosate was detected in dry garbanzo beans.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Dry Garbanzo Beans are sold under different brands and described as follows: -Bulk 2000 lbs. Totes. -CBP brand 25# Paper Bags 035084321925. -FIESTA brand 25# Paper Bags 035084225070. -Home Pride brand 50# Paper Bags 035084225070. -WinCo 24/1 lbs Small Pack 070552704305.

Quantity: 68,933 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.

Bulk 2000 lbs. Totes: LOT # 11/8/2019. CBP brand 25# Paper Bags 035084321925: LOT #: 10/25/2019, 11/06/2019, and 11/12/2019. FIESTA brand 25# Paper Bags 035084225070: LOT #: 11/14/2019 and 12/19/19. Home Pride brand 50# Paper Bags 035084225070: LOT #: 11/14/2019. WinCo 24/1 lbs Small Pack 070552704305: LOT #: NOV 12 2020

Where it was sold

Arizona California Idaho Oregon Texas Washington

FDA's distribution note: distributed in AZ, CA, ID, OR, TX, WA and in Canada.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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
Columbia Bean & Produce, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 6, 2020
In FDA report of
Jan 22, 2020
Terminated
Mar 5, 2020
FDA recall number
F-0519-2020 · event 84646
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.