Olam Food Ingredients Recall: Product may contain Salmonella
United States
TerminatedClass I
- Company
- Olam Food Ingredients
- Product
- Onion Powder Premium, 44.9 and 50 lb. fiber bags sold as bul…
- Recall date
- May 19, 2023
- Terminated
- May 24, 2024
- Source
- FDA
Reason for recall
Product may contain Salmonella
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Onion Powder Premium, 44.9 and 50 lb. fiber bags sold as bulk ingredient | Not published in this source record | 42,764 lbs. | Lot numbers: 2271957A00, 2234957A04, 2278953A09, 2237953A16 |
Distribution
- Product shipped to Canada
- Arkansas
- and Illinois
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0977-2023
- Event ID
- 92405
- Status
- Terminated
- Classification
- Class I
- Company
- Olam Food Ingredients
- Product description
- Onion Powder Premium, 44.9 and 50 lb. fiber bags sold as bulk ingredient
- Quantity
- 42,764 lbs.
- Reason
- Product may contain Salmonella
- Recall initiation date
- May 19, 2023
- Report date
- June 14, 2023
- Classification date
- Not published in this source record
- Termination date
- May 24, 2024
- Distribution pattern
- Product shipped to Canada, Arkansas, and Illinois
- UPC, lot, and code information
- Lot numbers: 2271957A00, 2234957A04, 2278953A09, 2237953A16
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Olam Food Ingredients
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
