FDA product code RHP: Uv Lamp, Germicidal
RHP is the FDA product code for uv lamp, germicidal. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 8 recalls for RHP devices, 8 initiated in the last five years.
Definition
An ultraviolet wavelength noncoherent light source intended for use in general purpose, germicidal systems.
Classification
| Field | Value |
|---|---|
| Device name | Uv Lamp, Germicidal |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for RHP devices
8 product recalls in 8 recall events; 8 initiated in the last five years and 8 still open. Most recent: 2026-03-06.
| Year | Recalls |
|---|---|
| 2021 | 1 |
| 2022 | 4 |
| 2025 | 1 |
| 2026 | 2 |
Frequently asked questions
What is FDA product code RHP?
RHP is the FDA product code for uv lamp, germicidal. It is a Not classified device, reviewed by the Unknown panel.
What device class is RHP?
Not classified.
Have RHP devices been recalled?
Yes: 8 product recalls across 8 recall events; the most recent began 2026-03-06.
Next steps
- Run an FDA pathway report with predicate devices for product code RHP
- Run a recall and safety report across every RHP manufacturer
- Watch product code RHP for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.