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Randall Foods, Inc.

Complete recall history across all FDA and CPSC categories — 8 total recalls

Randall Foods, 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 (8)

FDA food safety enforcement actions by Randall Foods, Inc.

Date Product Reason Class
May 19, 2021 RANDALL BLACK BEANS 48OZ glass jars UPC 070095000605; RANDALL BLACK BEANS 24O... Lack of functioning Temperature Indicating Devices in retorts Class II
May 19, 2021 RANDALL PINTO BEANS 48OZ glass jars UPC 070095000209; RANDALL PINTO BEANS 24O... Lack of functioning Temperature Indicating Devices in retorts Class II
May 19, 2021 RANDALL GARBANZO BEANS 24OZ glass jars UPC 070095000711; RANDALL GARBANZO BEA... Lack of functioning Temperature Indicating Devices in retorts Class II
May 19, 2021 RANDALL ULITMATE 4-BEAN MIX 48OZ glass jars UPC 070095000902 Lack of functioning Temperature Indicating Devices in retorts Class II
May 19, 2021 RANDALL KIDNEY BEANS 48OZ glass jars UPC 070095000308; RANDALL KIDNEY BEANS 2... Lack of functioning Temperature Indicating Devices in retorts Class II
May 19, 2021 RANDALL NAVY BEANS 48OZ glass jars UPC 070095000506; RANDALL NAVY BEANS 15.4O... Lack of functioning Temperature Indicating Devices in retorts Class II
May 19, 2021 RANDALL GREAT NORTHERN BEANS 48OZ glass jar UPC 070095000100; RANDALL GREAT N... Lack of functioning Temperature Indicating Devices in retorts Class II
May 19, 2021 RANDALL MIXED BEANS 48OZ glass jars UPC 070095000407; RANDALL MIXED BEANS 24O... Lack of functioning Temperature Indicating Devices in retorts 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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