MEAL SIMPLE RED LENTIL DAL SOUP NET WT. 16 OZ (1 LB) 454g UPC 1 97870 07333 0 MADE WITH PRIDE AND CARE FOR H-E-B-, SAN A
Summary
The FDA issued a Class II for MEAL SIMPLE RED LENTIL DAL SOUP NET WT. 16 OZ (1 LB) 454g UPC 1 97870 07333 0 MA by Bakkavor. Reason: Undeclared Milk. Wrong product in container..
Details
Source
Food Recall
External ID
H-0457-2026
Action Date
2026-01-28
Status
Ongoing
Category
food
Product Description
MEAL SIMPLE RED LENTIL DAL SOUP NET WT. 16 OZ (1 LB) 454g UPC 1 97870 07333 0 MADE WITH PRIDE AND CARE FOR H-E-B-, SAN ANTONIO, TEXAS 78204
Lot/Code Info: Lot: 882428 Best By Date 1/11/2026
Quantity Affected: 291cs/6/1lb cups
Reason for Recall
Undeclared Milk. Wrong product in container.
Distribution
All product was shipped to one distribution center in TX.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-08
Company
Charlotte, NC
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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Bakkavor 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 (Bakkavor) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bakkavor have FDA actions?
Bakkavor 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-0457-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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