Sunrise Medical (US) LLC recalls Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of assistin

Recalled August 4, 2021 · FDA recall Z-2158-2021 · Sunrise Medical (US)

Hazard

The seating system unexpectedly detached, which resulted in the seating system falling to the ground, causing injury. · FDA Class II

Units

4,741 device

Sold at

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.

Description

The seating system unexpectedly detached, which resulted in the seating system falling to the ground, causing injury.

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(s)

Sunrise Medical (US) LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →