Drug recall
"DING CHUAN TANG" or also labeled as "Breathe Smooth" Product is "DING CHUAN TANG" or also labeled as "Breathe…
FDA recall event 47757 · Class I, Class II, Class III · Jen-On Herbal Science International Inc.
Key facts
| Event ID | 47757 |
|---|---|
| Recall numbers | F-1520-2011, F-1521-2011, F-1522-2011, F-1523-2011, F-1524-2011, F-1525-2011, F-1526-2011, F-1527-2011, F-1528-2011, F-1529-2011, F-1530-2011, F-1531-2011 |
| Recalling firm | Jen-On Herbal Science International Inc. |
| Product type | Food |
| Products | "DING CHUAN TANG" or also labeled as "Breathe Smooth" Product is "DING CHUAN TANG" or also labeled as "Breathe Smooth" and it is packaged in a hard plastic white colored bottle with sealed twist cap…, "DU HOU JI SHENG TANG" or also labeled as "Du Huo Joint Relief" Product is "DU HOU JI SHENG TANG" or also labeled as "Du Huo Joint Relief" is packaged in a hard plastic white colored bottle with twist…, "FANG FENG TONG SHENG SAN" Product is "FANG FENG TONG SHENG SAN" and it is packaged in a hard plastic white colored bottle with twist cap which has a protective seal wrapped around its cap that reads…, "FENG SHI ZHI TONG WAN" labeled in Chinese and "Joint Relief" labeled in English Product is labeled "FENG SHI ZHI TONG WAN" labeled in Chinese and "Joint Relief" labeled in English on the retail…, "GUO MIN BI YAN WAN" Product is "GUO MIN BI YAN WAN" and it is packaged in a hard plastic white colored bottle with twist cap which has a protective seal wrapped around its cap that reads in part… and 7 more |
| Classification | Class I, Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The product is misbranded in that it claimed to contain ephedra as an ingredient on the label when in fact FDA's analysis was unable to detect this trace amount., The recall was initiated because the dietary supplement contains aristolochic acid and therefore may present a serious health hazard to consumers., The recall was initiated because the dietary supplement contains ephedrine and therefore… |
| Initiation date | Apr 7, 2008 |
| Termination date | Jul 19, 2012 |
| City | City of Industry |
| State | CA |
| Country | United States |
| FEI number | 3006205973 |
At a glance
- 10–99 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports