FDA Recall United States Terminated Historical recordClass II
T & R Enterprises USA, Inc.
- Product
- Vegetable eggroll 2 oz. and 3 oz.
- Published
- December 25, 2019
- Distribution
- Distributed to food service distributors…
T & R Enterprises USA, Inc. Recall: Produced and packaged under insanitary conditions
United States
TerminatedClass II
- Company
- T & R Enterprises USA, Inc.
- Product
- Crab Rangoon 1.0 oz.
- Recall date
- October 21, 2019
- Terminated
- January 23, 2020
- Source
- FDA
Reason for recall
Produced and packaged under insanitary conditions
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Crab Rangoon 1.0 oz. | Not published in this source record | 600/100/1 oz/eggrolls/cases | 080119 to 092619 |
Distribution
- Distributed to food service distributors in California and Michigan.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0349-2020
- Event ID
- 84121
- Status
- Terminated
- Classification
- Class II
- Company
- T & R Enterprises USA, Inc.
- Product description
- Crab Rangoon 1.0 oz.
- Quantity
- 600/100/1 oz/eggrolls/cases
- Reason
- Produced and packaged under insanitary conditions
- Recall initiation date
- October 21, 2019
- Report date
- December 25, 2019
- Classification date
- Not published in this source record
- Termination date
- January 23, 2020
- Distribution pattern
- Distributed to food service distributors in California and Michigan.
- UPC, lot, and code information
- 080119 to 092619
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 84121 with 1 other product entry in Public Health Trace.
Responsible company: T & R Enterprises USA, Inc.
Other recalls from T & R Enterprises USA, Inc.
FDA Recall United States Terminated Historical recordClass II
T & R Enterprises USA, Inc.
- Product
- Vegetable egg rolls packaged either 96 3oz per case or 120 2…
- Published
- August 25, 2021
- Distribution
- Distributed to restaurants in the St. Lo…
FDA Recall United States Terminated Historical recordClass II
T & R Enterprises USA, Inc.
- Product
- Vegetable eggroll 2 oz. and 3 oz.
- Published
- December 25, 2019
- Distribution
- Distributed to food service distributors…
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.
