Zippie Voyage — Class II medical device recall Z-2157-2021
Terminated recall by Sunrise Medical (US) LLC, reported 2021-08-04, distributed nationwide. The seating system unexpectedly detached, which resulted in the seating system falling to the ground, causing
| Recall number | Z-2157-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sunrise Medical (US) LLC, Fresno, CA, United States |
| Recall initiated | 2021-07-08 |
| Classified | 2021-07-28 |
| Reported by FDA | 2021-08-04 |
| Terminated | 2025-03-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, BH, CA, CH, CN, CZ, DE, ES, FR, GB, HK, ID, IL, IN, IT, JP, NL, NO, PL, QA, SA, SE, SG |
| Quantity | 9,865 devices |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00016958053647 |
| Serial numbers | ZV1-007000-ZV1-016036, ZV18-000001-ZV18-002220, ZV18-02062 |
| Model numbers | EIZ16 |
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.
Reason for recall
The seating system unexpectedly detached, which resulted in the seating system falling to the ground, causing injury.
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-2157-2021. 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.