SECOND NATURE KETO CRUNCH SMART MIX, 10-ounce retail-sized plastic pouch, UPC 077034013405, 6-10oz units per case.
Summary
The FDA issued a Class II for SECOND NATURE KETO CRUNCH SMART MIX, 10-ounce retail-sized plastic pouch, UPC 07 by SECOND NATURE BRAND. Reason: The product may contain undeclared allergens (cashews, pistachios), and dried cherries..
Details
Source
Food Recall
External ID
H-0905-2026
Action Date
2026-06-10
Status
Ongoing
Category
food
Product Description
SECOND NATURE KETO CRUNCH SMART MIX, 10-ounce retail-sized plastic pouch, UPC 077034013405, 6-10oz units per case.
Lot/Code Info: Best if Used By: 2/12/2027
Quantity Affected: 24,756 (10-oz pouch) total units
Reason for Recall
The product may contain undeclared allergens (cashews, pistachios), and dried cherries.
Distribution
Distributed nationwide in retail stores and through online orders.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-01
Company
Madison Heights, MI
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 166 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (SECOND NATURE BRAND) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SECOND NATURE BRAND have FDA actions?
This is the only FDA action we have on record for SECOND NATURE BRAND in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0905-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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