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3Cs Organics Llc

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

3Cs Organics Llc 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 3Cs Organics Llc

Date Product Reason Class
May 18, 2017 HIPP Anti-Reflux AR Bio-Spezialnahrung, 500g (4/case) The product is not FDA approved and not all products are labeled in English. Class II
May 18, 2017 HIPP Organic Comb Hungry Infant Milk, 800g (4bx/case), HIPP Organic Comb Firs... The product is not FDA approved and not all products are labeled in English. Class II
May 18, 2017 HIPP Tetrapack-Liquid , Single Serve Combiotik Hungry Infant, 200mL (6pk/24ca... The product is not FDA approved and not all products are labeled in English. Class II
May 18, 2017 Lebenswert Bioland Anfangsmilch1, 500g (4/case), Lebenswert Bioland Folgemilc... The product is not FDA approved and not all products are labeled in English. Class II
May 18, 2017 HOLLE Bio Lait Pour Nourrissons Au Lait De Chevre, Zuigelingenmelk OP Geitenm... The product is not FDA approved and not all products are labeled in English. Class II
May 18, 2017 Topfer Lactana Bio 1 Anfangsmilch, 600g (3/case), Topfer Lactana Bio 2, Bio F... The product is not FDA approved and not all products are labeled in English. Class II
May 18, 2017 HIPP Bio Combiotik 1, Canister, 900g (4/case), HIPP Bio Combiotik 2, Canist... The product is not FDA approved and not all products are labeled in English. Class II
May 18, 2017 HOLLE Bio Zulgelingen Opvolgmelk 2, (3/case), HOLLE Bio Lait de suite, 2, 400... The product is not FDA approved and not all products are labeled in English. Class II
May 18, 2017 HIPP HA Combiotik HA 1, 500g (4/case), HIPP Combiotik HA 2, 500g (4/case), HA... The product is not FDA approved and not all products are labeled in English. 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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