Starwest Botanicals, Inc
Complete recall history across all FDA and CPSC categories — 10 total recalls
Starwest Botanicals, 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 (10)
FDA food safety enforcement actions by Starwest Botanicals, Inc
| Date | Product | Reason | Class |
|---|---|---|---|
| Apr 2, 2021 | Starwest Botanicals Item#: 209617-34, Item# 209617-31 Wood Betony Herb C/S... | Presence of E. coli species | Class II |
| Oct 16, 2020 | Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia Distributed in ... | Direct customer tested product upon receipt and had a positive result for Sal... | Class I |
| Oct 16, 2020 | Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia 1 lb. and 4 oz. ... | Direct customer tested product upon receipt and had a positive result for Sal... | Class II |
| Mar 6, 2018 | Cardamom Pods Green Whole Organic Sold in 25 lb. bulk boxes and 1 lb. ret... | Customer notified firm after they received a positive result for Salmonella o... | Class I |
| Jan 14, 2015 | BAM124 Chili Powder Salt Free | Notified by immediate supplier of recall of ground cumin from Turkey due to t... | Class I |
| Jan 14, 2015 | BAM150 Caribbean Jerk Seasoning | Notified by immediate supplier of recall of ground cumin from Turkey due to t... | Class I |
| Jan 14, 2015 | BAM142 Blue Cheese Jalapeno Steak | Notified by immediate supplier of recall of ground cumin from Turkey due to t... | Class I |
| Jan 14, 2015 | BAM023 Sweet Curry Powder | Notified by immediate supplier of recall of ground cumin from Turkey due to t... | Class I |
| Jan 14, 2015 | 205190-50 Cumin Seed Powder | Notified by immediate supplier of recall of ground cumin from Turkey due to t... | Class I |
| Dec 30, 2014 | Ground cumin seed; Received in 50 lb. bags Shipped in 25# bags Country of ... | Firm was notified by supplier of ground cumin that it may contain peanut pro... | 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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