Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 00514 0. Taste of Maui S
Summary
The FDA issued a Class II for Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57 by J2C Hawaii LLC. Reason: Ingredients List declares peanut but the Contains statement does not declare peanut.
Details
Source
Food Recall
External ID
H-0523-2026
Action Date
2026-03-04
Status
Terminated
Category
food
Product Description
Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 00514 0. Taste of Maui Snacks dba of J2C Hawaii, LLC PO Box 1023, Wailuku HI 96793. The product label is read in parts: ***INGREDIENTS: Sugar***Whey Powder, Nonfat Milk Powder, Soy Lecithin***Peanut Butter (peanuts, peanut oil***), Pretzels (wheat flour***buttermilk solids***CONTAINS MILK AND SOY ***May contain wheat, peanuts and tree nuts***"
Lot/Code Info: All packages with BB 11/26 or before
Quantity Affected: 300 units
Reason for Recall
Ingredients List declares peanut but the Contains statement does not declare peanut
Distribution
Distributed in HI only.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-01-30
Company
Wailuku, HI
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 27 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 (J2C Hawaii LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does J2C Hawaii LLC have FDA actions?
This is the only FDA action we have on record for J2C Hawaii LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0523-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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