Zip International Group LLC.

Complete recall history across all FDA and CPSC categories — 6 total recalls

Zip International Group LLC. 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 (6)

FDA food safety enforcement actions by Zip International Group LLC.

Date Product Reason Class
Dec 16, 2013 Fosforel Atlantika Herring Fillet in Oil (200 g) Product of Russia Imported ... NYSDAM analysis has revealed the presence of Listeria monocytogenes in two sa... Class I
Nov 25, 2013 Fosforel Atlantika Herring Fillet in Oil 14.1 oz. (400 g) Product of Russia I... ZIP INTERNATIONAL GROUP LLC is recalling herring fillet in oil (FOSFOREL, AT... Class I
Aug 1, 2013 Baltic Sprats in Spicy Brine Net Wt. 15.8 oz. Prod. of Latvia Distributed by... Baltic Sprats in Spicy Brine may be contaminated with Listeria monocytogenes. Class I
Jul 19, 2013 FOSFOREL brand Herring Fillet in Oil 400 gram (14 oz.) in plastic packaging ... The product was found to contain Listeria monocytogenes based on sampling and... Class I
May 17, 2013 Marmalade Fonariky Net 105.8 oz (3 kg) Product of Russia upc 460161417406 Marmalade contains undeclared colors and dyes. Class II
Apr 26, 2013 Kaija Ivasi Lightly Salted Herring Fillets in Oil UPC 3585600709 Kaija Ivasi lightly salted herring does not meet water phase salt standard of... 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.

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