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G.O. Fresh

Complete recall history across all FDA and CPSC categories — 9 total recalls

G.O. Fresh 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 (9)

FDA food safety enforcement actions by G.O. Fresh

Date Product Reason Class
Sep 13, 2012 SYSCO Imperial 9498072 FRUIT W/GOLD PINEAPPLE KIT 4/1.5# 130250 BEST BY 9/16/... G.O. Fresh in Minnesota is voluntarily recalling specific cut items that cont... Class I
Sep 13, 2012 SYSCO Imperial 2232734 4/5# FRUIT VARIETY CHUNK 3/4" 130249 & 130250 BEST BY ... G.O. Fresh in Minnesota is voluntarily recalling specific cut items that cont... Class I
Sep 13, 2012 SYSCO Imperial 4835718 30/4.5 OZ FRUIT MIX CANT/PINE/REDGRAPES 130249 & 1302... G.O. Fresh in Minnesota is voluntarily recalling specific cut items that cont... Class I
Sep 13, 2012 SYSCO Imperial 5370204 30/4.5 OZ/ ,30# FRUIT VARIETY GARDEN-TO-GO 130249 & 1... G.O. Fresh in Minnesota is voluntarily recalling specific cut items that cont... Class I
Sep 13, 2012 Cut Cantaloupe: G.O Fresh: 0379729 4/5# CANTALOUPE CHUNKS (PACKER) 130250 B... G.O. Fresh in Minnesota is voluntarily recalling specific cut items that cont... Class I
Sep 13, 2012 SYSCO Imperial 1/5# PAIL MELON MIX HONEY-CANT W/ GRAPE 7225071 1/5#MELON W/GR... G.O. Fresh in Minnesota is voluntarily recalling specific cut items that cont... Class I
Sep 13, 2012 SYSCO Imperial 47340104/5# FRUIT MIX W/ORANGE WEDGES 130250 BEST BY 9/16/12,... G.O. Fresh in Minnesota is voluntarily recalling specific cut items that cont... Class I
Sep 13, 2012 Mixed Fruit w/ Grapes: SYSCO Imperial 1210321 4/5# FRUIT MIX CHUNK W/GRAPES 1... G.O. Fresh in Minnesota is voluntarily recalling specific cut items that cont... Class I
Sep 13, 2012 SYSCO Imperial 6520795 1/5# FRUIT MIX CHUNKS 3/4" 130249 & 130250 BEST BY 9/1... G.O. Fresh in Minnesota is voluntarily recalling specific cut items that cont... 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.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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