Class ITerminatedVoluntary: Firm initiated
Caraluzzi's Markets: food recall F-0747-2025
Caraluzzi's Markets of BETHEL, CT recalled Caraluzzi's Italian Style Seafood Burgers, 8oz; INGREDIENTS: Cod, Salmon, Shrimp, Scallops, Onions, Olive Oil, White… Reason: Product contains undeclared egg. The FDA listed it as Class I in its Enforcement Report dated May 7, 2025; distribution: Connecticut.
Record status as published: Terminated (terminated Aug 5, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Caraluzzi's Italian Style Seafood Burgers, 8oz; INGREDIENTS: Cod, Salmon, Shrimp, Scallops, Onions, Olive Oil, White Wine, Parsley, Sodium Caseinate (A Milk Derivative), Spices, Garlic, Salt, Paprika, Enzyme.; CONTAINS: Crustacean Shellfish, Fish, Milk; Distributed by Caraluzzi's Markets, Bethel, CT 06801; UPC: 0 95864 80008 8
- Product quantity
- 79 units
- Reason for recall
- Product contains undeclared egg.
- Codes, lots and dates on the package
- Expiration: 1/16/2026
- Distribution pattern
- CT
- Recalling firm
- Caraluzzi's Markets, BETHEL, CT
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Apr 2, 2025 |
| Classified by the FDA | Apr 30, 2025 |
| Published in the Enforcement Report | May 7, 2025 |
| Terminated | Aug 5, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0747-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.