Full Moon Fish Tuna Steaks Recalled for Incorrect Label Information
ALFA INTERNATIONAL SEAFOOD INC is recalling Full Moon Fish Tuna Steaks because the labels contain incorrect manufacturer numbers, pack dates, and expiration dates.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is for minor labeling errors (incorrect dates and numbers) with no reported health hazards or illnesses, fitting the criteria for a moderate severity score.
Plain-English summary
ALFA INTERNATIONAL SEAFOOD INC is voluntarily recalling approximately 6,830 pounds of Full Moon Fish Tuna Steaks, Skinless, Boneless, IVP, Size: 8 oz, Net Weight 5 lbs. The recall was initiated because the product labels contain incorrect information, specifically listing the wrong manufacturer number, pack date, and expiration date.
The affected product was distributed only within the United States. The production date is listed as 02/04/2019, and the expiration date is listed as 02/04/2021. The recall is classified as Class II by the FDA.
Consumers who have purchased this product should check their labels for the incorrect information and stop using the product. They should contact the recalling firm for further instructions or a refund.
The recalled product
- Product
- Full Moon Fish Tuna Steaks, Skinless, Boneless, IVP, Size: 8 oz, Net Weight 5 lbs
- Manufacturer
- ALFA INTERNATIONAL SEAFOOD INC
- Category
- Food — Seafood
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Production Date: 02/04/2019 Expiry Date: 02/04/2021
Distribution
Distribution scope not specified by the agency.
Related recalls
Same manufacturer · ALFA INTERNATIONAL SEAFOOD INC
See all →- SevereAlfa International Seafood Recalls Yellowfin Tuna Loins Due to Scombroid Poisoning
FDA (Food) · 2019-10-02
Same hazard · mis labeling
See all →- HighByron White Herbal Supplement Recalled for Undeclared Walnut Allergen
FDA (Food) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02