RegWardenFDA facility compliance records
Recall

Class II — Sunrise Medical (US) LLC

Recalling firmSunrise Medical International Inc.
Registered facilitySUNRISE MEDICAL INTERNATIONAL INC. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonThere 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.
ProductSunrise 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.
Quantity316 units in US, 29 units international
DistributionWorldwide Distribution-USA (nationwide) and the countries of Canada, Australia, Hong Kong, and China.
Initiated2013-11-11
Classified2013-12-05
Terminated2014-03-18
Recall numberZ-0453-2014
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Sunrise Medical (US) LLC (Z-0453-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/66896/

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