CAMPOMEX USA CORP Recall: Cilantro tested by imports but not released from was found positive for Cyclospora. Importer mistakenly took one pallet from the lot on hold and distributed it.
United States
TerminatedClass II
- Company
- CAMPOMEX USA CORP
- Product
- Campomex USA fresh cilantro: 5 dozens (60) per box.
- Recall date
- August 29, 2018
- Terminated
- November 29, 2018
- Source
- FDA
Reason for recall
Cilantro tested by imports but not released from was found positive for Cyclospora. Importer mistakenly took one pallet from the lot on hold and distributed it.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Campomex USA fresh cilantro: 5 dozens (60) per box. | Not published in this source record | 56 boxes | no codes |
Distribution
- CA only
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1968-2018
- Event ID
- 80968
- Status
- Terminated
- Classification
- Class II
- Company
- CAMPOMEX USA CORP
- Product description
- Campomex USA fresh cilantro: 5 dozens (60) per box.
- Quantity
- 56 boxes
- Reason
- Cilantro tested by imports but not released from was found positive for Cyclospora. Importer mistakenly took one pallet from the lot on hold and distributed it.
- Recall initiation date
- August 29, 2018
- Report date
- September 26, 2018
- Classification date
- Not published in this source record
- Termination date
- November 29, 2018
- Distribution pattern
- CA only
- UPC, lot, and code information
- no codes
- 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: CAMPOMEX USA CORP
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 |
|---|---|
| California | 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.
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