Taylor Farms Pacific Inc. (MacArthur Facility)
Complete recall history across all FDA and CPSC categories — 5 total recalls
Taylor Farms Pacific Inc. (MacArthur Facility) 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 (5)
FDA food safety enforcement actions by Taylor Farms Pacific Inc. (MacArthur Facility)
| Date | Product | Reason | Class |
|---|---|---|---|
| Oct 10, 2018 | Raley's Country Macaroni Salad labeled as Raley's Country Potato Salad; 32 oz... | Country Macaroni Salad was labeled as Country Potato Salad and does not decla... | Class II |
| Nov 19, 2016 | Taylor Farms Veggie & Hummus Bistro Box: Baby Carrots, Hummus Dip, Grape T... | Firm was notified by supplier that the hummus included in their vegetable and... | Class I |
| Dec 10, 2014 | Citizen Chef Organic Superfood Salad- 4 Organic Salads. Power Greens, Walnut... | Undeclared Milk on individual units, outer packaging is labeled correctly. | Class II |
| Sep 12, 2014 | Signature Cafe SWY Sicilian Vegetable Salad 2CT Kit Pack Size: 2-6.75 lb ba... | Firm was notified by supplier that specific lots of "expo fresh" Roma tomatoe... | Class I |
| Sep 12, 2014 | CST Roma Tomatoes Whole Roma 1/25# Origin: USA Keep Refrigerated UPC: 400... | Firm was notified by supplier that specific lots of "expo fresh" Roma tomatoe... | Class I |
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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