GARBANZO BEANS, SPROUTS FARMERS MARKET, Net Wt 16oz (1 LB) 454g units, 12 units / case. UPC 6 46670-51757 0. Distribut
Summary
The FDA issued a Class III for GARBANZO BEANS, SPROUTS FARMERS MARKET, Net Wt 16oz (1 LB) 454g units, 12 units by Trinidad Benham Corp. Reason: This recall has been initiated due to detection of glyphosate residues above tolerance..
Details
Source
Food Recall
External ID
F-1291-2023
Action Date
2023-08-02
Status
Terminated
Category
food
Product Description
GARBANZO BEANS, SPROUTS FARMERS MARKET, Net Wt 16oz (1 LB) 454g units, 12 units / case. UPC 6 46670-51757 0. Distributed by Sprouts Farmers Market, Phoenix, AZ 85054.
Lot/Code Info: BEST IF USED BY 20JAN24Y
Quantity Affected: 112 Cases (12 units / case)
Reason for Recall
This recall has been initiated due to detection of glyphosate residues above tolerance.
Distribution
CA
Type: Voluntary: Firm initiated
Recall Initiated: 2023-06-22
Company
Denver, CO
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 48 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Trinidad Benham Corp has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Trinidad Benham Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Trinidad Benham Corp have FDA actions?
Trinidad Benham Corp has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1291-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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