CLASS II Food recall · Reported 10 Dec 2025 · FDA Enforcement Report
Onion granules (irradiated) recalled by Laiwu Manhing Vegetables
Laiwu Manhing Vegetables Fruits is recalling Onion granules (irradiated), distributed in California. The recall was initiated on 5 Nov 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-0232-2026
- FDA event ID
- 97954
- Recalling firm
- Laiwu Manhing Vegetables Fruits, Shangdong
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 5 Nov 2025
- FDA classified
- 3 Dec 2025
- Reported
- 10 Dec 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Foreign Material
- Product category
- Onions
Timeline
| 5 Nov 2025 | Recall initiated by company | |
| 3 Dec 2025 | Classified by FDA | +28 days |
| 10 Dec 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
foreign objects (black plastic planting film) in granulated onion powder
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Onion granules (irradiated) ; 55 lbs carton Item# 5358
Where it was distributed
CA
Questions about this recall
Why was it recalled?
foreign objects (black plastic planting film) in granulated onion powder
Which lots are affected?
Lot# 21S066251458-1, Best before date: Feb.16,2027
Where was it sold?
CA
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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