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Ocean Group Inc.

Complete recall history across all FDA and CPSC categories — 7 total recalls

Ocean Group Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Food Recalls (7)

FDA food safety enforcement actions by Ocean Group Inc.

Date Product Reason Class
Nov 1, 2024 SALMON BAKKAFROST FAROE ISLANDS 5/6KG FR FRO F LB SALMON NORWAY 6/7KG FR NOR ... Potential for contamination of Listeria monocytogenes. Environmental sample c... Class II
Dec 29, 2023 202225 SALMON BAKKA FROST FILLET 6/7KG FR FRO F LB 202002 SALMON BAKKAFROST ... Potential L. mono contamination as a result of FDA environmental sampling rev... Class I
Dec 29, 2023 201000 TUNA, HAWAII #1 USA W LB 201002 TUNA HAWAII #1 USA W LB 201200 TUNA ... Potential L. mono contamination as a result of FDA environmental sampling rev... Class I
Dec 16, 2015 Masago Lake Smelt Roe 6 oz. UPC Code:4866010101 Product contains undeclared soy and wheat. Class I
Jun 2, 2012 Large IQF Oysters, 6 x 4 lb/cs Ocean Group is recalling tiny IQF oysters, large IQF oysters, and half shelf ... Class II
Jun 2, 2012 half shell Oysters, 144pc/cs Ocean Group is recalling tiny IQF oysters, large IQF oysters, and half shell ... Class II
Jun 2, 2012 Tiny IQF Oysters, 40pk/cs, 8oz. Ocean Group is recalling tiny IQF oysters, large IQF oysters, and half shell ... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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