CLASS II Device recall · Reported 11 Dec 2013 · FDA Enforcement Report
Sunrise Zippie Voyage, Chair with Casters recalled
Sunrise Medical is recalling Sunrise Zippie Voyage, Chair with Casters, Early Intervention Device (Stroller), distributed nationwide in the US. The recall was initiated on 11 Nov 2013 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0453-2014
- FDA event ID
- 66896
- Recalling firm
- Sunrise Medical, Fresno, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 11 Nov 2013
- FDA classified
- 5 Dec 2013
- Reported
- 11 Dec 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Foreign Material
- Device type
- Other Medical Devices
Timeline
| 11 Nov 2013 | Recall initiated by company | |
| 5 Dec 2013 | Classified by FDA | +24 days |
| 11 Dec 2013 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
There is a remote possibility for the plastic latch to deform over the lifetime of use. When this happens there is the possibility for the seat to become dislodged from the base. And when not using the positioning strap, there is a risk that the occupant could slide out of the seat and sustain injury.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Sunrise Brand Zippie Voyage, Chair with Casters, Early Intervention Device (Stroller), Model: EIZ14; Product is manufactured and distributed by Sunrise Medical (US) LLC., Fresno, CA. Used by a person to move from one place to another while sitting.
Where it was distributed
Worldwide Distribution-USA (nationwide) and the countries of Canada, Australia, Hong Kong, and China.
Questions about this recall
Why was it recalled?
There is a remote possibility for the plastic latch to deform over the lifetime of use. When this happens there is the possibility for the seat to become dislodged from the base. And when not using the positioning strap, there is a risk that the occupant could slide out of the seat and sustain injury.
Which lots are affected?
Serial Numbers: ZV-001563 ,ZV-001672 ,ZV-001691 ,ZV-001737 ,ZV-001740 ,ZV-001423 ,ZV-001537 ,ZV-001557 ,ZV-001604 ,ZV-001746 ,ZV-001749 ,ZV-001761 ,ZV-001669 ,ZV-001682 ,ZV-001722 ,ZV-001755 ,ZV-001711 ,ZV-001415 ,ZV-001634 ,ZV-001716 ,ZV-001615 ,ZV-001521 ,ZV-001589 ,ZV-001617 ,ZV-001618 ,ZV-001627 ,ZV-001683 ,ZV-001702 ,ZV-001763 ,ZV-001773 ,ZV-001491 ,ZV-001531 ,ZV-001534 ,ZV-001562 ,ZV-001560 ,ZV-001569 ,ZV-001575 ,ZV-001720 ,ZV-001772 ,ZV-001635 ,ZV-001659 ,ZV-001777 ,ZV-001712 ,ZV-001487 ,ZV-001526 ,ZV-001574 ,ZV-001759 ,ZV-001595 ,ZV-001555 ,ZV-001603 ,ZV-001775 ,ZV-001520 ,ZV-001485 ,ZV-001519 ,ZV-001460 ,ZV-001687 ,ZV-001515 ,ZV-001614 ,ZV-001465 ,ZV-001742 ,ZV-001767 ,ZV-001685 ,ZV-001628 ,ZV-001785 ,ZV-001407 ,ZV-001408 ,ZV-001507 ,ZV-001658 ,ZV-001663 ,ZV-001511 ,ZV-001532 ,ZV-001545 ,ZV-001778 ,ZV-001568 ,ZV-001585 ,ZV-001607 ,ZV-001631 ,ZV-001629 ,ZV-001650 ,ZV-001654 ,ZV-001675 ,ZV-001717 ,ZV-001769 ,ZV-001430 ,ZV-001570 ,ZV-001559 ,ZV-001475 ,ZV-001488 ,ZV-001489 ,ZV-001490 ,ZV-001542 ,ZV-001578 ,ZV-001583 ,ZV-001656 ,ZV-001728 ,ZV-001714 ,ZV-001652 ,ZV-001653 ,ZV-001536 ,ZV-001676 ,ZV-001355 ,ZV-001366 ,ZV-001483 ,ZV-001594 ,ZV-001701 ,ZV-001709 ,ZV-001554 ,ZV-001735 ,ZV-001463 ,ZV-001638 ,ZV-001580 ,ZV-001695 ,ZV-001726 ,ZV-001443 ,ZV-001474 ,ZV-001486 ,ZV-001508 ,ZV-001598 ,ZV-001606 ,ZV-001608 ,ZV-001692 ,ZV-001696 ,ZV-001782 ,ZV-001619 ,ZV-001664 ,ZV-001424 ,ZV-001433 ,ZV-001451 ,ZV-001457 ,ZV-001493 ,ZV-001512 ,ZV-001516 ,ZV-001543 ,ZV-001564 ,ZV-001581 ,ZV-001590 ,ZV-001602 ,ZV-001613 ,ZV-001641 ,ZV-001667 ,ZV-001671 ,ZV-001668 ,ZV-001680 ,ZV-001679 ,ZV-001684 ,ZV-001751 ,ZV-001593 ,ZV-001756 ,ZV-001535 ,ZV-001470 ,ZV-001539 ,ZV-001565 ,ZV-001624 ,ZV-001662 ,ZV-001752 ,ZV-001753 ,ZV-001647 ,ZV-001670 ,ZV-001704 ,ZV-001747 ,ZV-001660 ,ZV-001681 ,ZV-001783 ,ZV-001431 ,ZV-001434 ,ZV-001447 ,ZV-001482 ,ZV-001524 ,ZV-001550 ,ZV-001553 ,ZV-001586 ,ZV-001677 ,ZV-001734 ,ZV-001750 ,ZV-001770 ,ZV-001774 ,ZV-001784 ,ZV-001632 ,ZV-001459 ,ZV-001533 ,ZV-001518 ,ZV-001541 ,ZV-001538 ,ZV-001620 ,ZV-001467 ,ZV-001454 ,ZV-001546 ,ZV-001566 ,ZV-001477 ,ZV-001705 ,ZV-001505 ,ZV-001718 ,ZV-001719 ,ZV-001504 ,ZV-001609 ,ZV-001762 ,ZV-001724 ,ZV-001573 ,ZV-001600 ,ZV-001665 ,ZV-001694 ,ZV-001745 ,ZV-001517 ,ZV-001636 ,ZV-001582 ,ZV-001597 ,ZV-001612 ,ZV-001623 ,ZV-001439 ,ZV-001710 ,ZV-001754 ,ZV-001771 ,ZV-001510 ,ZV-001513 ,ZV-001523 ,ZV-001540 ,ZV-001599 ,ZV-001601 ,ZV-001640 ,ZV-001661 ,ZV-001699 ,ZV-001727 ,ZV-001766 ,ZV-001441 ,ZV-001764 ,ZV-001506 ,ZV-001744 ,ZV-001715 ,ZV-001757 ,ZV-001571 ,ZV-001674 ,ZV-001655 ,ZV-001414 ,ZV-001633 ,ZV-001732 ,ZV-001458 ,ZV-001509 ,ZV-001693 ,ZV-001547 ,ZV-001551 ,ZV-001639 ,ZV-001686 ,ZV-001725 ,ZV-001466 ,ZV-001649 ,ZV-001700 ,ZV-001438 ,ZV-001588 ,ZV-001730 ,ZV-001529 ,ZV-001530 ,ZV-001591 ,ZV-001626 ,ZV-001469 ,ZV-001468 ,ZV-001576 ,ZV-001579 ,ZV-001587 ,ZV-001596 ,ZV-001630 ,ZV-001689 ,ZV-001707 ,ZV-001713 ,ZV-001723 ,ZV-001736 ,ZV-001738 ,ZV-001410 ,ZV-001690 ,ZV-001484 ,ZV-001616 ,ZV-001729 ,ZV-001765 ,ZV-001556 ,ZV-001452 ,ZV-001478 ,ZV-001637 ,ZV-001657 ,ZV-001642 ,ZV-001651 ,ZV-001525 ,ZV-001522 ,ZV-001548 ,ZV-001698 ,ZV-001584 ,ZV-001739 ,ZV-001741 ,ZV-001622 ,ZV-001697 ,ZV-001743 ,ZV-001760 ,ZV-001678 ,ZV-001527 ,ZV-001528 ,ZV-001721 ,ZV-001788 ,ZV-001605 ,ZV-001572 ,ZV-001446 ,ZV-001549 ,ZV-001748 ,ZV-001409 ,ZV-001703 ,ZV-001644 ,ZV-001708 ,ZV-001444 ,ZV-001473 ,ZV-001645 ,ZV-001442 ,ZV-001552 ,ZV-001648 ,ZV-001787 ,ZV-001437 ,ZV-001643 ,ZV-001688 ,ZV-001706 ZV-001611.
Where was it sold?
Worldwide Distribution-USA (nationwide) and the countries of Canada, Australia, Hong Kong, and China.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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|---|---|---|---|---|---|
| Device | CLASS II | Zippie Voyage, early intervention stroller recalled | Sunrise Medical | Other | Nationwide |
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