Dermalight 80 Model Number UVB-080 — Class III medical device recall Z-1778-2013
Terminated recall by National Biological Corp, reported 2013-07-31, distributed nationwide. The incorrect manual may have been packaged with this product. UVB-080 devices may have included the manual fo
| Recall number | Z-1778-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | National Biological Corp, Beachwood, OH, United States |
| Recall initiated | 2013-04-09 |
| Classified | 2013-07-19 |
| Reported by FDA | 2013-07-31 |
| Terminated | 2014-02-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, CA, MX, MY |
| Quantity | 124 units |
| Lot numbers | 7839, 7951 |
| Serial numbers | D80-12748, D80-12871 |
| Model numbers | UVB-080 |
Product
Dermalight 80 Model Number UVB-080, one unit per box. The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for diagnosed skin disorders such as Psoriasis and Vitiligo.
Reason for recall
The incorrect manual may have been packaged with this product. UVB-080 devices may have included the manual for a UVA-083 device.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1778-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.