Lutosa S.A. Recall: Potential foreign object; plastic and rubber pieces.
United States
TerminatedClass II
- Company
- Lutosa S.A.
- Product
- Lutosa Foodservice Quality Plain Mashed Produced in Belgi…
- Recall date
- September 24, 2018
- Terminated
- April 18, 2019
- Source
- FDA
Reason for recall
Potential foreign object; plastic and rubber pieces.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Lutosa Foodservice Quality Plain Mashed Produced in Belgium 2.5 kg/5.5 lb | Not published in this source record | 8640 kg | Lot Numbers: L8056 24 20 L8057 24 14 L8057 24 15 L8057 24 16 L8057 24 17 L8057 24 18 L8057 24 19 |
Distribution
- U.S. distribution to NV. Foreign distribution to Japan.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0057-2019
- Event ID
- 81109
- Status
- Terminated
- Classification
- Class II
- Company
- Lutosa S.A.
- Product description
- Lutosa Foodservice Quality Plain Mashed Produced in Belgium 2.5 kg/5.5 lb
- Quantity
- 8640 kg
- Reason
- Potential foreign object; plastic and rubber pieces.
- Recall initiation date
- September 24, 2018
- Report date
- October 31, 2018
- Classification date
- Not published in this source record
- Termination date
- April 18, 2019
- Distribution pattern
- U.S. distribution to NV. Foreign distribution to Japan.
- UPC, lot, and code information
- Lot Numbers: L8056 24 20 L8057 24 14 L8057 24 15 L8057 24 16 L8057 24 17 L8057 24 18 L8057 24 19
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Lutosa S.A.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Nevada | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
