CLASS III Food recall · Reported 4 Mar 2026 · FDA Enforcement Report
Mung Beans recalled by Lubna Quality Products
Lubna Quality Products is recalling Mung Beans, distributed in Louisiana, Texas. The recall was initiated on 15 Jan 2026 and the FDA has classified it as Class III.
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-0524-2026
- FDA event ID
- 98327
- Recalling firm
- Lubna Quality Products, Houston, TX
- Brand
- Mung
- Classification
- Class III
- Status
- Completed
- Recall initiated
- 15 Jan 2026
- FDA classified
- 24 Feb 2026
- Reported
- 4 Mar 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Packaging Defects
- Product category
- Beans & Lentils
Timeline
| 15 Jan 2026 | Recall initiated by company | |
| 24 Feb 2026 | Classified by FDA | +40 days |
| 4 Mar 2026 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Presence of Thiamethoxam-PESTICIDE
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Mung Beans packaged in 4lb polybags; 6-4lb bags per carton
Where it was distributed
Texas and Louisiana
Questions about this recall
Is Mung Beans recalled?
Yes. Lubna Quality Products recalled Mung Beans on 15 Jan 2026. The recall is Class III and its status is Completed. Recall number H-0524-2026.
Why was it recalled?
Presence of Thiamethoxam-PESTICIDE
Which lots are affected?
Lot: JAN 2025, Batch KI/050122
Where was it sold?
Texas and Louisiana
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 III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 21 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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|---|---|---|---|---|---|
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