H-E-B Corpus Christi Operations Recall: Foreign material, possibly corn husk, present in corn tortillas.
United States
TerminatedClass II
- Company
- H-E-B Corpus Christi Operations
- Product
- HEB Homestyle White Corn Tortillas, 12 Count and 30 Count pa…
- Recall date
- December 9, 2016
- Terminated
- March 1, 2017
- Source
- FDA
Reason for recall
Foreign material, possibly corn husk, present in corn tortillas.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| HEB Homestyle White Corn Tortillas, 12 Count and 30 Count packaged in clear plastic bags. | Not published in this source record | 10,941 units | UPC codes: 4122058841 and 4122058742; Best by dates Dec 17 and Dec 18, 2016 |
Distribution
- Texas
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1244-2017
- Event ID
- 75927
- Status
- Terminated
- Classification
- Class II
- Company
- H-E-B Corpus Christi Operations
- Product description
- HEB Homestyle White Corn Tortillas, 12 Count and 30 Count packaged in clear plastic bags.
- Quantity
- 10,941 units
- Reason
- Foreign material, possibly corn husk, present in corn tortillas.
- Recall initiation date
- December 9, 2016
- Report date
- January 18, 2017
- Classification date
- Not published in this source record
- Termination date
- March 1, 2017
- Distribution pattern
- Texas
- UPC, lot, and code information
- UPC codes: 4122058841 and 4122058742; Best by dates Dec 17 and Dec 18, 2016
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: H-E-B Corpus Christi Operations
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?
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