Junebar Chocolate Cherry All Natural Snack Bar; INGREDIENTS: ORGANIC ALMOND BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORG
Summary
The FDA issued a Class I for Junebar Chocolate Cherry All Natural Snack Bar; INGREDIENTS: ORGANIC ALMOND BUTT by Juniper Granola, LLC. Reason: Products contain undeclared milk and soy..
Details
Source
Food Recall
External ID
H-0543-2026
Action Date
2026-03-11
Status
Terminated
Category
food
Product Description
Junebar Chocolate Cherry All Natural Snack Bar; INGREDIENTS: ORGANIC ALMOND BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN CHOCOLATE CHIPS (ORGANIC CANE SUGAR, UNSWEETENED CHOCOLATE, COCOA BUTTER), DRIED CHERRIES, ALMONDS; OAT FLOUR, COCOA POWDER, ORANGE ZEST, VANILLA EXTRACT (VANILLA BEAN EXTRACTIVES IN WATER, ALCOHOL), FLAX, CINNAMON, SEA SALT, BAKING POWDER; ALLERGEN WARNING: CONTAINS TREE NUTS (ALMOND, COCONUT), PRODUCED ON EQUPMENT ALSO HANDLING PEANUT, SESAME. PRODUCED IN A FACILITY THAT ALSO PROCESES GLUTEN PRODUCTS. KEEP REFRIGERATED; UPC: 8 60012 38462 4
Lot/Code Info: Lot L1300, including L1300A and L1300B. Lot number is stamped on the back, near the bottom of each individual bar pouch.
Quantity Affected: 1800 bars total
Reason for Recall
Products contain undeclared milk and soy.
Distribution
New York
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-11
Company
Rochester, NY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 26 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Juniper Granola, LLC has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Juniper Granola, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Juniper Granola, LLC have FDA actions?
Juniper Granola, LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0543-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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