boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels NET WT 26.5 OZ (1.66 LB) 750g Ingredients: Organic wheat fl
Summary
The FDA issued a Class II for boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels NET WT 26.5 OZ (1.66 by Boichik Bagels, Inc.. Reason: Undeclared allergen, sesame..
Details
Source
Food Recall
External ID
H-1133-2026
Action Date
2026-07-01
Status
Ongoing
Category
food
Product Description
boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels NET WT 26.5 OZ (1.66 LB) 750g Ingredients: Organic wheat flour ... Contains Wheat Topped flavors may additionally contain ... sesame seeds ... Best by SE 26 26 UPC: 850016588067
Lot/Code Info: Best by: MAY 25 26, JUN 20 26, JUL 15 26, AUG 23 26, SE 26 26
Quantity Affected: 426 packages (6 bagels/package)
Reason for Recall
Undeclared allergen, sesame.
Distribution
Domestic: CA Foreign: Not applicable
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-22
Company
Berkeley, CA
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 58 food recalls issued in the same week, part of 92 food-related FDA actions this month.
Boichik Bagels, Inc. has 3 FDA actions in our database, including 3 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 (Boichik Bagels, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Boichik Bagels, Inc. have FDA actions?
Boichik Bagels, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1133-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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