Swanson Health Products, Inc
Complete recall history across all FDA and CPSC categories — 6 total recalls
Swanson Health Products, 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 (6)
FDA food safety enforcement actions by Swanson Health Products, Inc
| Date | Product | Reason | Class |
|---|---|---|---|
| Mar 4, 2022 | Swanson Ultra: Vitamin B12 Methylcobalamin High Absorption 60 serving per co... | Dietary supplement may contain potential metal shavings greater than or equal... | Class II |
| Sep 13, 2018 | Swanson Ultra, Himalayan Crystal Salt, #SWU403, Net Wt. 35.27 oz. (2.2 lbs) (... | Himalayan Crystal Salt may contain metal wire pieces. | Class II |
| Jul 28, 2014 | Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net w... | Swanson Certified Organic Carob Powder, item number SWF115 is being recalled ... | Class I |
| Mar 28, 2014 | Swanson Full Spectrum Cilantro (Coriander) Herbal Supplement, 60 capsules, 42... | The contract manufacturer has notified Swanson Health Products that Swanson F... | Class I |
| Sep 26, 2013 | Swanson, Premium Brand, Full Spectrum Black Cumin Seed (Nigella Sativa) Diet... | Swanson Health Products is recalling two lots of Swanson Premium Full Spectr... | Class III |
| Oct 23, 2012 | Swanson Organic, 100% Certified Organic Fennel Seed, Net Wt 6 oz (45 grams), ... | This is to inform you of a product recall involving 2 lots of Swanson Organic... | Class III |
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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