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International Sprout Holding Inc.

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

International Sprout Holding 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 International Sprout Holding Inc.

Date Product Reason Class
Oct 6, 2021 SunGarden Mung Bean Sprouts 5lb & 10lb packaged in clear plastic bag in ... Product tested positive for Listeria monocytogenes Class I
Dec 30, 2019 Clover seed in 55 lb. multi-layered white paper bags, 40 bags to a pallet. Possible contamination with E. Coli. Class I
Dec 30, 2019 Clover seed in 50 lb. woven poly bags, 40 bags to a pallet. Possible contamination with E. Coli. Class I
Mar 31, 2016 ALFALFA SEED, NET WT. 50 LB. International Specialty Supply LLC, Cookeville, TN One sample taken were positive for Salmonella Poly B Class I
Nov 4, 2014 Alfalfa Seed in plastic lined bags labeled in part *** VNS Alfalfa, NET WT. ... A sample of one lot of product tested positive for salmonella. Class I
Oct 27, 2014 Alfalfa seed: Organic, Alfalfa, NOP Oregon Tilth, Net Wt. 55 LB, Internation... A sample taken by FDA of one lot of alfalfa seed tested positive for Salmonella Class I
Aug 1, 2014 Clover, Crimson, Net Wt. 50 LB. PRODUCT OF USA, International Specialty Suppl... Crimson Clover seed tested positive for Listeria Monocytogenes 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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