CLASS II ONGOING Food recall · Reported 28 Jan 2026 · FDA Enforcement Report
Meal Simple Red Lentil Dal Soup recalled by Bakkavor
Bakkavor is recalling Meal Simple Red Lentil Dal Soup, distributed in Texas. The recall was initiated on 8 Dec 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0457-2026
- FDA event ID
- 98121
- Recalling firm
- Bakkavor, Charlotte, NC
- Brand
- Meal Simple
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 8 Dec 2025
- FDA classified
- 3 Feb 2026
- Reported
- 28 Jan 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Milk
- Product category
- Soup
Timeline
| 8 Dec 2025 | Recall initiated by company | |
| 28 Jan 2026 | Published in enforcement report | +51 days |
| 3 Feb 2026 | Classified by FDA | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared Milk. Wrong product in container.
Product as listed by the FDA
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
Where it was distributed
All product was shipped to one distribution center in TX.
Stores named: H-E-B
Questions about this recall
Why was it recalled?
Undeclared Milk. Wrong product in container.
Which lots are affected?
Lot: 882428 Best By Date 1/11/2026
Where was it sold?
All product was shipped to one distribution center in TX.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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