Premium Food Jordan Almonds, packed in 2.0 oz and 3.5 oz clear flexible plastic packaging.
Summary
The FDA issued a Class II for Premium Food Jordan Almonds, packed in 2.0 oz and 3.5 oz clear flexible plastic by Bader Enterprises, Inc.. Reason: Contains undeclared allergen (wheat) and colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake)..
Details
Source
Food Recall
External ID
H-0538-2026
Action Date
2026-03-11
Status
Ongoing
Category
food
Product Description
Premium Food Jordan Almonds, packed in 2.0 oz and 3.5 oz clear flexible plastic packaging.
Lot/Code Info: Size: 2.0 oz Net Wt. 57 grams, Lot/Unit Numbers: 6, BEST BY: DEC 2028, UPC Codes: 015750199171 Size: 3.5 oz Net Wt. 99 grams, Lot/Unit Numbers: 6, BEST BY: DEC 2028, UPC Codes: 015750299215
Quantity Affected: 60 lbs.
Reason for Recall
Contains undeclared allergen (wheat) and colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
Distribution
NJ, NY
Type: Voluntary: Firm initiated
Recall Initiated: 2026-01-16
Company
Brooklyn, NY
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 26 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Bader Enterprises, Inc. has 2 FDA actions in our database, including 2 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 (Bader Enterprises, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bader Enterprises, Inc. have FDA actions?
Bader Enterprises, Inc. 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-0538-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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