Stop using nowMedical device recall · FDA · Published July 8, 2021
Sunrise Medical Zippie Voyage Stroller Recall: Seating System Detaches Causing Injury
Sunrise Medical recalls Zippie Voyage strollers with model EIZ16/EIZ18 that may detach unexpectedly, causing injury. Affected units include specific serial ranges. Stop using immediately to prevent falls.
“Sunrise Medical Zippie Voyage Stroller Recall: Seating System Detaches Causing Injury.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62233-sunrise-medical-zippie-voyage-stroller-recall-seating-system-detaches-causing. Based on FDA recall #Z-2157-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2157-2021%22&limit=1).
The FDA announced on July 8, 2021, that Sunrise Medical (US) LLC voluntarily recalled Zippie Voyage early intervention strollers because the seating system can unexpectedly detach and fall. The agency said the hazard caused injuries.
How to tell if you have it
Brand: Sunrise Medical
Product: Zippie Voyage, early intervention stroller
Model Numbers: EIZ16; EIZ18
UPC: 00016958053647
Serial Numbers: ZV1-007000-ZV1-016036; ZV18-000001-ZV18-002220; and ZV18-02062
The hazard
The FDA said the seating system unexpectedly detached, which resulted in the seating system falling to the ground, causing injury.
Context
GovInfoNow's records show Sunrise Medical (US) LLC has 1 other recall on record since 2020-02-13. On 2020-02-13, the company recalled Q700M Powered Wheelchairs due to a programming error risk. Other recent recalls of similar products include Medline Bariatric Rollator Recall (2026-08-14) and Medline medical kits recall (2026-02-27).
How to tell if you have this one
Check for model numbers EIZ16 or EIZ18 on the stroller. Look for serial numbers starting with ZV1-007000 to ZV1-016036 or ZV18-000001 to ZV18-002220.
Brand
Sunrise Medical
Product
Zippie Voyage, early intervention stroller
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
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.
Recall number
Product, codes & lots
Quantity
Z-2157-2021
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.; Model Numbers: EIZ16; EIZ18; GTIN Number: 00016958053647 Serial Numbers: ZV1-007000-ZV1-016036; ZV18-000001-ZV18-002220; and ZV18-02062
9,865 devices
Z-2158-2021
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.; Model Numbers: EIZ14; Serial Numbers: ZV-001340 through ZV-006153
4,741 device
Based on the official FDA remedy
What to do — step by step
Stop Using Now
Immediately stop using the stroller if it has model numbers EIZ16 or EIZ18 and the specified serial numbers.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 50 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA 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…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA terminated this recall 3.7 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2157-2021 (July 8, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2157-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.