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Class IITerminated in FDA datasetRecall initiated Jan 10, 2023

Superior Fresh Lettuce Blend

Recalling firm: Superior Fresh, LLC

Why it was recalled

Foreign material (small glass particles)

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: Sep 15, 2023.

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

ProductSuperior Fresh Lettuce Blend Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Green Oak Leaf, Butter lettuce, Arugula, spinach. Keep Refrigerated. Packaged under the following Names and sizes: 1. Spring Mix Family Pack Net Wt. 8 oz (227g) UPC 8 50038-27428 3. 2. Spring Mix, Net Wt 4 oz. (113g) UPC 8 57871-00888 4. Grown for you By: Superior Fresh LLC, Hixton, WI 54635
Package size8 oz
UPC850038274283, 857871008884

FDA code information

Best By: 1/20, Best By: 1/21, and Best By: 1/23

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

Full FDA record and distribution details

Original product description

Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Green Oak Leaf, Butter lettuce, Arugula, spinach. Keep Refrigerated. Packaged under the following Names and sizes: 1. Spring Mix Family Pack Net Wt. 8 oz (227g) UPC 8 50038-27428 3. 2. Spring Mix, Net Wt 4 oz. (113g) UPC 8 57871-00888 4. Grown for you By: Superior Fresh LLC, Hixton, WI 54635

Extracted codes and context

TypeCode / valueContext
UPC850038274283following Names and sizes: 1. Spring Mix Family Pack Net Wt. 8 oz (227g) UPC 8 50038-27428 3. 2. Spring Mix, Net Wt 4 oz. (113g) UPC 8 57871-00888 4. Grown for you By: Superior Fresh LLC, Hixton, WI 546
UPC8578710088848 oz (227g) UPC 8 50038-27428 3. 2. Spring Mix, Net Wt 4 oz. (113g) UPC 8 57871-00888 4. Grown for you By: Superior Fresh LLC, Hixton, WI 54635

Original FDA recall reason

Foreign material (small glass particles)

Recall details

Recall number
F-0304-2023
Event ID
91496
FDA status
Terminated
Initiated
Jan 10, 2023
Reported
Jan 25, 2023
Classified
Jan 19, 2023
Terminated
Sep 15, 2023
Quantity
1516 cases (total)
Location
Hixton, WI, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

IN, PA, VA, WI

FDA source record · F-0304-2023

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

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