PHAROS Excimer Laser — Class II medical device recall Z-2123-2014
Terminated recall by Ra Medical Systems Inc, reported 2014-08-06, distributed nationwide. RA Medical Systems is recalling the PHAROS EX-308 Excimer Laser because there is a possibility that the laser
| Recall number | Z-2123-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ra Medical Systems Inc, Carlsbad, CA, United States |
| Recall initiated | 2014-06-30 |
| Classified | 2014-07-28 |
| Reported by FDA | 2014-08-06 |
| Terminated | 2014-09-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | KR, KW, SA |
| Quantity | 435 units |
| Serial numbers | 1000, 1001, 1002, 1003, 1004, 1005, 1006, 1007, 1008, 1009, 1010, 1014, 1015, 1016, 1017, 1018, 1021, 1022, 1023, 1024, 1025, 1027, 1028, 1029, 1030 and 364 more |
| Model numbers | EX-308UVB |
Product
PHAROS Excimer Laser, Model No. EX-308 UVB phototherapy for the treatment of psoriasis, vitiligo, atopic dermatitis and leukoderma
Reason for recall
RA Medical Systems is recalling the PHAROS EX-308 Excimer Laser because there is a possibility that the laser may calibrate with the iris closed.
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-2123-2014. 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.