Drug recall
Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (100-3B)
FDA recall event 84117 · Class II · Basic Reset Inc.
Key facts
| Event ID | 84117 |
|---|---|
| Recall numbers | Z-0348-2020 |
| Recalling firm | Basic Reset Inc. |
| Product type | Devices |
| Products | Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (100-3B) |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | FDA Requested |
| Reason for recall | FDA determined that marketing claims surrounding product rendered product a medical device which was adulterated and misbranded. |
| Initiation date | Oct 18, 2019 |
| Report date | Nov 20, 2019 |
| City | Hendersonville |
| State | TN |
| Country | United States |
| FEI number | 3007197806 |
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: