Sea Queen 9/15oz Encrusted Tilapia Fillets, Item Number: B1290
Recalling firm: High Liner Foods Inc.
Why it was recalled
Product may contain undeclared milk.
The exact product
Sea Queen 9/15oz Encrusted Tilapia Fillets, Item Number: B1290
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Lot Number: 0027021220; 0027023220; 0027018211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221
| Type | Code / value | Context |
|---|---|---|
| lot | 0027018120 | Lot Number: 0027021220; 0027023220; 0027018211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221 |
| lot | 0027018211 | Lot Number: 0027021220; 0027023220; 0027018211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221 |
| lot | 0027018220 | Lot Number: 0027021220; 0027023220; 0027018211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221 |
| lot | 0027021120 | Lot Number: 0027021220; 0027023220; 0027018211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221 |
| lot | 0027021220 | Lot Number: 0027021220; 0027023220; 0027018211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221 |
| lot | 0027023220 | Lot Number: 0027021220; 0027023220; 0027018211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221 |
| lot | 0027038220 | Number: 0027021220; 0027023220; 0027018211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221 |
| lot | 0027038221 | 021220; 0027023220; 0027018211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221 |
| lot | A0027018220 | 023220; 0027018211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221 |
| lot | FB0027038221 | 18211; 0027018220; 0027018120; 0027021120; 0027038220; 0027038221; A0027018220; FB0027038221 |
Recall details
- Recall number
- F-2660-2017
- Event ID
- 77489
- FDA status
- Terminated
- Initiated
- Jun 9, 2017
- Reported
- Aug 23, 2017
- Classified
- Aug 15, 2017
- Terminated
- Dec 14, 2017
- Quantity
- 693,408 cases (total for all products)
- Location
- Portsmouth, NH, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
Nationwide
FDA source record · F-2660-2017
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.