Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Gr
Summary
The FDA issued a Class II for Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf, Green Leaf, Gree by Superior Fresh, LLC. Reason: Foreign material (small glass particles).
Details
Source
Food Recall
External ID
F-0302-2023
Action Date
2023-01-25
Status
Terminated
Category
food
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, Kale, Spinach, Mustard, Mizuna, Pax Choi. Keep Refrigerated. Packaged under the following Names and sizes: 1. Spring Mix, Net Wt 4 oz. (113g) UPC 8 57871-00882 2. 2. Midwest Medley, Net Wt 4 oz. (113g) UPC 8 57871-00882 2. 3. Midwest Meledy Family Pack 8 oz. (227g), UPC 8 50038-27426 9 Grown for you By: Superior Fresh LLC, Hixton, WI 54635
Lot/Code Info: 1. Best By: 1/19, Best By: 1/20, Best By: 1/21, and Best By: 1/23. 2. Best By: 1/19, Best By: 1/20, Best By: 1/21, and Best By: 1/23. 3. Best By: 1/21 and Best By: 1/23.
Quantity Affected: 1516 cases (total)
Reason for Recall
Foreign material (small glass particles)
Distribution
IN, PA, VA, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-10
Company
Hixton, WI
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 84 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Superior Fresh, LLC has 6 FDA actions in our database, including 6 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Superior Fresh, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Superior Fresh, LLC have FDA actions?
Superior Fresh, LLC has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0302-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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