Check the Batch
Class ITerminated in FDA datasetRecall initiated Jan 22, 2016

Leafy Romaine Salad

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.

ProductLeafy Romaine Salad, 10 oz. 10 oz. bag, - Walmart; Leafy Romaine, 10 oz. bag - Kroger Romaine Blend - 10 oz. bag - Kroger 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 size10 oz

FDA code information

All packaged salads with manufacturing code beginning with the letter A. Walmart - production code 3141; Kroger- production code: 3005, 3011 (leafy romaine)

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

Full FDA record and distribution details

Original product description

Leafy Romaine Salad, 10 oz. 10 oz. bag, - Walmart; Leafy Romaine, 10 oz. bag - Kroger Romaine Blend - 10 oz. bag - Kroger 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.

Extracted codes and context

TypeCode / valueContext
production code3005g with the letter A. Walmart - production code 3141; Kroger- production code: 3005, 3011 (leafy romaine)
production code3011 the letter A. Walmart - production code 3141; Kroger- production code: 3005, 3011 (leafy romaine)

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-0647-2016
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-0647-2016

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

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