Drug recall
Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York
FDA recall event 65441 · Class I · Bethel Nutritional Consulting, Inc
Key facts
| Event ID | 65441 |
|---|---|
| Recall numbers | D-921-2013 |
| Recalling firm | Bethel Nutritional Consulting, Inc |
| Product type | Drugs |
| Products | Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Marketed Without An Approved NDA/ANDA: FDA analysis found this product contained undeclared sibutramine and phenolphthalein, two active ingredients that were once marketed in the U.S. but removed due… |
| Initiation date | Jun 11, 2013 |
| Report date | Sep 4, 2013 |
| Termination date | Jun 27, 2018 |
| City | New York |
| State | NY |
| Country | United States |
| FEI number | 3010099772 |
At a glance
- 1–9 Products in this recall
- 1–9 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 · Source date: