The Recall Desk
SevereFDA (Devices)·Z-2158-2021·Announced 2021-08-04

Zippie Voyage Early Intervention Stroller Seating System Detachment

Sunrise Medical is recalling the Zippie Voyage early intervention stroller due to unexpected seating system detachment that can cause falls and injury. Approximately 4,741 devices are affected worldwide.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: FDA Class II medical device with documented injury resulting from an unexpected seating system detachment. The hazard affects vulnerable users (young children and small adults) through a sudden, uncontrolled failure mode.

Plain-English summary

Sunrise Medical (US) LLC is recalling the Zippie Voyage early intervention stroller, a manually operated mobility assistance device designed for use by caregivers with children and small adults not to exceed 75 pounds. Approximately 4,741 devices are affected.

The seating system can unexpectedly detach from the stroller, causing it to fall to the ground. This hazard has resulted in injury.

The affected devices are Model Number EIZ14 with serial numbers ZV-001340 through ZV-006153. The recalled strollers have been distributed worldwide and throughout the United States.

The recalled product

Product
Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of assisting a disabled person while providing supportive elements for assisted transportation and seating for a child or small adult not to exceed 75 pounds.
Manufacturer
Sunrise Medical (US) LLC
Category
Medical Device — Mobility Device
Hazard
Affected units
4,741

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Model Numbers: EIZ14
  • Serial Numbers: ZV-001340 through ZV-006153

Distribution

Distributed nationwide across the United States.

The notice also names 51 states specifically:

Part of a larger recall action

This product is one of 2 recalled by Sunrise Medical (US) LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Related recalls

Same manufacturer · Sunrise Medical (US) LLC

See all →

Same hazard · seat detachment

See all →