Class II — MERCHSOURCE LLC
| Recalling firm | Merchsource LLC |
|---|---|
| Registered facility | MERCHSOURCE LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Excessive ultraviolet-C radiation |
| Product | The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range. |
| Quantity | N/A |
| Distribution | US Nationwide Distribution |
| Initiated | 2022-08-01 |
| Classified | 2022-09-06 |
| Recall number | Z-1661-2022 |
| Initiation | FDA Mandated |
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 — MERCHSOURCE LLC (Z-1661-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90799/
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