Class II — JK Products & Services, Inc
| Recalling firm | JK Products & Services |
|---|---|
| Registered facility | JK PRODUCTS & SERVICES, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The Beauty Angel was marketed without a 510k. |
| Product | BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use. |
| Quantity | 598 units |
| Distribution | Worldwide Distribution - USA (nationwide) and Canada |
| Initiated | 2012-05-07 |
| Classified | 2012-08-10 |
| Terminated | 2015-01-07 |
| Recall number | Z-2183-2012 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — JK Products & Services, Inc (Z-2183-2012).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/61855/
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