FDA Device recall Z-2123-2014
PHAROS Excimer Laser, Model No. EX-308 UVB phototherapy for the treatment of psoriasis, vitiligo, atopic dermatitis and leukoderma
- FDA Device
- Class II
- terminated
- Published 2014-08-06
On 2014-08-06 the FDA classified a Class II recall of PHAROS Excimer Laser, Model No. EX-308 UVB phototherapy for the treatment of psoriasis, vitiligo, atopic dermatitis and leukoderma by Ra Medical Systems, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2123-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-30 |
| Published | 2014-08-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ra Medical Systems |
| Distribution | US |
Product
PHAROS Excimer Laser, Model No. EX-308 UVB phototherapy for the treatment of psoriasis, vitiligo, atopic dermatitis and leukoderma
Reason
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.
Identifiers
| code_info | Serial Numbers: 40 41 99 112 114 119 124 234 237 250 251 271 272 274 276 283 299 302 306 314 315…Serial Numbers: 40 41 99 112 114 119 124 234 237 250 251 271 272 274 276 283 299 302 306 314 315 316 319 321 323 324 325 326 329 333 337 350 351 352 356 357 358 359 360 382 383 394 396 397 398 400 402 404 405 407 409 411 414 417 418 419 420 421 423 424 428 430 431 441 450 455 457 459 460 462 463 464 465 467 471 475 476 480 482 483 484 486 488 490 491 494 495 496 497 500 505 507 509 512 516 518 519 525 526 527 528 529 531 532 533 534 535 537 538 539 541 543 546 550 552 553 554 555 556 557 559 560 561 562 563 565 566 567 570 571 572 573 574 576 579 580 582 583 585 586 588 589 591 592 593 594 595 597 598 599 600 601 602 603 604 605 606 609 610 614 615 617 622 623 624 628 629 631 632 633 635 636 637 638 639 644 645 646 647 648 649 654 655 656 657 659 661 662 663 664 665 667 668 669 672 673 674 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2123-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.