--- Organic Baby Carrots --- Organic Baby Carrots 25 Grimmway Farms; Organic Baby Carrots 25 Lbs. Grimmway Farms --- Bra
Summary
The FDA issued a Class I for --- Organic Baby Carrots --- Organic Baby Carrots 25 Grimmway Farms; Organic Bab by Grimmway Enterprises, Inc. dba Grimmway Farms. Reason: Potential contamination with E. coli O121:H19.
Details
Source
Food Recall
External ID
F-0359-2025
Action Date
2025-01-08
Status
Terminated
Category
food
Product Description
--- Organic Baby Carrots --- Organic Baby Carrots 25 Grimmway Farms; Organic Baby Carrots 25 Lbs. Grimmway Farms --- Brand --- Grimmway Farms
Lot/Code Info: 127734 127773 127830 127871 127875 127936 127975 127978 128036 128059 128063 128129 128133 128163 128238 128264 128291 128336 128383 128482
Quantity Affected: 21,094 cases
Reason for Recall
Potential contamination with E. coli O121:H19
Distribution
Distribution Centers located in U.S. States: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI U.S. Territories: Puerto Rico Foreign Countries: Canada, United Arab Emirates, Hong Kong, Columbia
Type: Voluntary: Firm initiated
Recall Initiated: 2024-11-16
Company
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Grimmway Enterprises, Inc. dba Grimmway Farms has 13 FDA actions in our database, including 13 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Grimmway Enterprises, Inc. dba Grimmway Farms) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Grimmway Enterprises, Inc. dba Grimmway Farms have FDA actions?
Grimmway Enterprises, Inc. dba Grimmway Farms has 13 FDA actions in our database, including 13 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0359-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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