T MARZETTI INNOVATION CENTER Recall: Undeclared Egg Allergen
United States
TerminatedClass I
- Company
- T MARZETTI INNOVATION CENTER
- Product
- Blanched Penne Rigati 8oz plastic bag 40 bags per case
- Recall date
- April 14, 2021
- Terminated
- June 11, 2021
- Source
- FDA
Reason for recall
Undeclared Egg Allergen
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Blanched Penne Rigati 8oz plastic bag 40 bags per case | Not published in this source record | 210 cases | Case Code 10219CPC Product Bag Codes 10219C1PC & 10219C2PC |
Distribution
- Product was sent to a single consignee located in San Bernardino
- CA. The consignee is a relabler/repacker who create Home Chief Meal Kits.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0487-2021
- Event ID
- 87736
- Status
- Terminated
- Classification
- Class I
- Company
- T MARZETTI INNOVATION CENTER
- Product description
- Blanched Penne Rigati 8oz plastic bag 40 bags per case
- Quantity
- 210 cases
- Reason
- Undeclared Egg Allergen
- Recall initiation date
- April 14, 2021
- Report date
- May 19, 2021
- Classification date
- Not published in this source record
- Termination date
- June 11, 2021
- Distribution pattern
- Product was sent to a single consignee located in San Bernardino, CA. The consignee is a relabler/repacker who create Home Chief Meal Kits.
- UPC, lot, and code information
- Case Code 10219CPC Product Bag Codes 10219C1PC & 10219C2PC
- 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: T MARZETTI INNOVATION CENTER
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 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.
