FDA Recall United States Terminated Historical recordClass II
Trident Seafoods Corporation
- Product
- Trident Seafoods Pacific Salmon Burgers (# 414469), frozen.…
- Published
- April 14, 2021
- Distribution
- distributed in Georgia, Florida and Texa…
Trident Seafoods Corporation Recall: Product may contain undeclared egg white.
United States
TerminatedClass I
- Company
- Trident Seafoods Corporation
- Product
- Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2…
- Recall date
- June 18, 2020
- Terminated
- November 19, 2020
- Source
- FDA
Reason for recall
Product may contain undeclared egg white.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution exclusively by Gordon Food Service Wyoming, MI 49509 | 93901-71212 | 50,550 lbs. | All product produced prior to 6/18/2020. Production Date is printed on the package. Lot Codes Effected: M828803 expiration date 10/15/2020 M904202 expiration date 02/11/2021 M916303 expiration date 06/12/2021 M935004 expiration date 12/16/2021 M016004 expiration date 06/08/2022 |
Distribution
- Nationwide in the following states: AL
- CT
- FL
- GA
- IL
- IN
- KY
- LA
- MA
- MD
- ME
- MI
- MO
- MS
- NC
- NH
- OH
- PA
- RI
- SC
- TN
- TX
- WI
- WV
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1019-2020
- Event ID
- 85893
- Status
- Terminated
- Classification
- Class I
- Company
- Trident Seafoods Corporation
- Product description
- Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution exclusively by Gordon Food Service Wyoming, MI 49509
- Quantity
- 50,550 lbs.
- Reason
- Product may contain undeclared egg white.
- Recall initiation date
- June 18, 2020
- Report date
- July 8, 2020
- Classification date
- Not published in this source record
- Termination date
- November 19, 2020
- Distribution pattern
- Nationwide in the following states: AL, CT, FL, GA, IL, IN, KY, LA, MA, MD, ME, MI, MO, MS, NC, NH, OH, PA, RI, SC, TN, TX, WI, WV
- UPC, lot, and code information
- UPC 93901-71212; All product produced prior to 6/18/2020. Production Date is printed on the package. Lot Codes Effected: M828803 expiration date 10/15/2020 M904202 expiration date 02/11/2021 M916303 expiration date 06/12/2021 M935004 expiration date 12/16/2021 M016004 expiration date 06/08/2022
- 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: Trident Seafoods Corporation
Other recalls from Trident Seafoods Corporation
FDA Recall United States Terminated Historical recordClass II
Trident Seafoods Corporation
- Product
- Kroger brand. Frozen non-ready to eat Alaskan Salmon Bites,…
- Published
- November 14, 2018
- Distribution
- Nationwide
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 |
|---|---|
| Alabama | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| North Carolina | 1 |
| New Hampshire | 1 |
| Ohio | 1 |
| Pennsylvania | 1 |
| Rhode Island | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Wisconsin | 1 |
| West Virginia | 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.
