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FDA source record Class II Terminated

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, Mus...

Recall Date: 2023-01-10 Recalling Firm: Superior Fresh, LLC Record Ref: F-0302-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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, Mus... and names Superior Fresh, LLC as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Superior Fresh, LLC
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2023-01-10
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Product Description & Identification

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

Reason for Recall / Hazard Identified

Foreign material (small glass particles)

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

IN, PA, VA, WI

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0302-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
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