# FDA recall Z-2157-2021

> **Sunrise Medical (US) LLC** · Class II · device recall initiated 2021-07-08.

## 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.

## Distribution

Worldwide distribution - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. The countries of United Kingdom, Germany, France, Canada, Italy, Netherlands, Poland, Czech Republic, Australia, Hong Kong, Japan, Qatar, Norway, United Arab Emirates, China, Saudi Arabia, Sweden, Switzerland, Spain, Indonesia, India, Singapore, Bahrain and Israel.

## Key facts

- **Recall number:** Z-2157-2021
- **Recalling firm:** Sunrise Medical (US) LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-08
- **Report date:** 2021-08-04
- **Termination date:** 2025-03-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fresno, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2157-2021

## Citation

> AI Analytics. FDA recall Z-2157-2021. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2157-2021. Source: US FDA. Licensed CC0.

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