Class ITerminated in FDA datasetRecall initiated Jan 22, 2016

Shredded Lettuce

Recalling firm: Dole Fresh Vegetables Inc

Why it was recalled

Dole is suspending operations and withdrawing all marketed Dole and private label salads produced at the Springfield OH facility. Products may be identified with a product code…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 23, 2016.

Check your package

Compare the exact product and package details with the label you have.

ProductShredded Lettuce , 11 oz. bag - Kroger Value Size Shredded Lettuce - 16 oz. bag - Dole; 1/4'' Shredded Lettuce-Dole brand Chopped lettuce 5 lb bag - Dole. All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand corner of the package.
Package size11 oz

FDA code information

All packaged salads with manufacturing code beginning with the letter A. Kroger production code - 3029. Dole production code - 157 (186 oz) 75 (5 lb. bag) and 72 (1/4')

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Shredded Lettuce , 11 oz. bag - Kroger Value Size Shredded Lettuce - 16 oz. bag - Dole; 1/4'' Shredded Lettuce-Dole brand Chopped lettuce 5 lb bag - Dole. All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand corner of the package.

Original FDA recall reason

Dole is suspending operations and withdrawing all marketed Dole and private label salads produced at the Springfield OH facility. Products may be identified with a product code beginning with the letter A in the upper right hand corner of the package.

Recall details

Recall number
F-0661-2016
Event ID
73128
FDA status
Terminated
Initiated
Jan 22, 2016
Reported
Mar 9, 2016
Classified
Feb 26, 2016
Terminated
Mar 23, 2016
Quantity
All product produced in the facility
Location
Monterey, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Nationwide and Canada

FDA source record · F-0661-2016

Data updated September 16, 2026. View official FDA data ↗

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