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Haig's Delicacies

Complete recall history across all FDA and CPSC categories — 4 total recalls

Haig's Delicacies 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 (4)

FDA food safety enforcement actions by Haig's Delicacies

Date Product Reason Class
Dec 21, 2012 Falafel with Tahini Sauce; nuggets of ground garbanzo beans with a rich, tan... State of CA inspection found four products do not declare allergy statements ... Class II
Dec 21, 2012 Tzatziki; Greek yogurt with cucumber and dill. sold in 8 oz retail and 5 lb ... State of CA inspection found four products that do not declare allergy statem... Class I
Dec 21, 2012 Tyropita; a triangular phyllo dough pastry with cheese filling. sold in 5 l... State of CA inspection found four products that do not declare allergy statem... Class I
Dec 21, 2012 Spanakopita; a triangular phyllo dough pastry with spinach and cheese filling... State of CA inspection found four products that do not declare allergy statem... 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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