Zippie Voyage Voyage; Voyage VIPRecalls & reported problems
Sunrise Medical (US) LLC · The Zippie Voyage® is a lightweight highly adjustable early intervention stroller. In addition to adjustable tilt and recline, the Voyage also features adjustable head supports, upper body supports and positioning straps. Comes with or without seating. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00016958053647), received between Sep 24, 2021 and Jan 31, 2024 — classified as 3 injuries, 6 malfunctions.
The most frequently reported specific device problem is “Misassembly by Users” (8 reports).
1 FDA recall record name this device's identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Recalls naming this device
- Jul 8, 2021Class IITerminated
The seating system unexpectedly detached, which resulted in the seating system falling to the ground, causing injury.
Z-2157-2021 · Root cause: Device Design · Recall details · FDA record ↗
Most reported problems
Device problems
- Misassembly by Users8
- Misassembled During Installation1
Patient problems
- Fall8
- Head Injury4
- Bruise/Contusion1
- Laceration(s)1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjuryJan 31, 2024Misassembled During Installation; Misassembled During Installation
A VOLUNTARY MEDWATCH REPORT (MW5149183) WAS RECEIVED DETAILING AN INCIDENT INVOLVING A ZIPPIE VOYAGE WHEELCHAIR WHERE THE SEAT BECAME DETACHED FROM THE BASE AND FLIPPED UPSIDE DOWN. THE END USER REPORTEDLY LANDED ON HIS HEAD. THE END USER ALLEGEDLY SUSTAINED BRUISING AND A NON-DESCRIPTIVE HEAD INJURY. THERE WAS NO INFORMATION PROVIDED REGARDING DIAGNOSIS OR TREATMENT.
Patient problems: Bruise/Contusion; Head Injury
MAUDE report 18619206 ↗InjuryDec 17, 2021Misassembly by Users; Misassembly by Users
THE DEALER DESCRIBES AN INCIDENT THAT OCCURRED WHERE A "BOY FELL OUT OF THE CHAIR" AND RECEIVED A CUT TO THE FOREHEAD THAT REQUIRED 8 STITCHES TO CLOSE. NO OTHER DESCRIPTION OF THE INCIDENT WAS PROVIDED.
Patient problems: Fall
MAUDE report 13028476 ↗MalfunctionDec 16, 2021Misassembly by Users; Misassembly by Users
THE CAREGIVER/MOTHER DESCRIBES AN INCIDENT THAT OCCURRED LAST SUMMER (A YEAR AGO) DURING WHICH THE LATCH ALLEGEDLY DIDN'T HOLD ALLOWING THE CHILD TO FALL OUT FACE FIRST ON THE CEMENT. THE CHILD WAS SEEN BY A PHYSICIAN AT THE TIME AND CONFIRMED NO CONCUSSION; HOWEVER, THE CHILD SUFFERED MINOR CUTS AND SCRAPES TO THEIR FACE AND NOSE. THE MOTHER CALLED IN TO CUSTOMER SERVICE DUE TO RECEIVING THE RECALL NOTIFICATION IN THE MAIL (RECALL NO. 88257).
Patient problems: Fall
MAUDE report 13022455 ↗MalfunctionDec 14, 2021Misassembly by Users; Misassembly by Users
THE CAREGIVER/MOTHER DESCRIBES AN INCIDENT THAT OCCURRED ON (B)(6) 2021 WHEN SHE REMOVED A DIAPER BAG FROM THE BACK OF THE CHAIR AND THE "SEATING CAME OFF." SHE DID NOT NOTICE ANY INJURY, HOWEVER, HER DAUGHTER HAS SEEN AN INCREASE IN SEIZURE ACTIVITY AND NEEDED TYLENOL "FOR PAIN" TO SLEEP. NO MEDICAL ATTENTION WAS SOUGHT AND THE MOTHER DOES NOT KNOW IF THIS CHANGE IS RELATED TO THE FALL. THE MOTHER COMPLAINS NO LONGER USING THE CHAIR AND HAVING IT STORED IN THE GARAGE DUE TO SAFETY CONCERNS. THE MOTHER CALLED IN TO CUSTOMER SERVICE DUE TO RECEIVING THE RECALL NOTIFICATION IN THE MAIL (RECALL NO. 88257).
Patient problems: Fall
MAUDE report 13002530 ↗MalfunctionDec 3, 2021Misassembly by Users; Misassembly by Users
THE CAREGIVER/MOTHER DESCRIBES AN INCIDENT THAT OCCURRED "ABOUT A YEAR AGO" WHEN HER SON (DATE UNSPECIFIED) WAS ROCKING BACK AND FORTH WHEN THE SEATING SYSTEM DETACHED FROM THE STROLLER BASE AND FELL TO THE GROUND. NO MEDICAL ATTENTION WAS SOUGHT ALTHOUGH MOTHER REPORTS A "BUSTED FACE." THE MOTHER HAS SINCE STOPPED USING THE STROLLER DUE TO THE REPORT THAT "THE STROLLER BASE IS TOO HEAVY TO LIFT INTO THE CAR." THE MOTHER CALLED IN TO CUSTOMER SERVICE DUE TO RECEIVING THE RECALL NOTIFICATION IN THE MAIL (RECALL NO. 88257).
Patient problems: Fall; Laceration(s)
MAUDE report 12927861 ↗MalfunctionDec 2, 2021Misassembly by Users; Misassembly by Users
THE CAREGIVER DESCRIBES THREE SEPARATE INCIDENTS, DATES UNSPECIFIED, WHERE THE STROLLER SEAT FELL FROM THE STROLLER BASE. THE LAST INCIDENT, THE DEALER REPORTS THAT THE SEATING SYSTEM "DID NOT LATCH AND FELL OFF THE BASE WITHOUT THE CHILD IN THE CHAIR." ALSO, "DEALER THINKS IT IS A LATCH FAILURE OR STRAP ISSUE;" HOWEVER, LATCH WAS NOT TESTED AND, IF INSPECTION WAS PERFORMED, IT WAS NOT DOCUMENTED. ALSO, PRODUCT WAS NOT RETURNED TO THE MANUFACTURER FOR TESTING. THE CAREGIVER, AFTER THE THIRD INCIDENT, STOPPED USING THE STROLLER. NO INJURIES ARE REPORTED.
Patient problems: Fall
MAUDE report 12921129 ↗MalfunctionNov 7, 2021Misassembly by Users; Misassembly by Users
THE CAREGIVER DESCRIBES TWO SEPARATE INCIDENTS, THE FIRST IN (B)(6) OF 2018 AND AGAIN IN 2019 (DATE UNKNOWN) WHERE THE STROLLER SEAT WAS NOT ADEQUATELY ATTACHED TO THE BASE AND THE SEAT FELL FROM THE STROLLER BASE. UPON BECOMING AWARE OF THE RECALL, THE CAREGIVER CONTACTED SUNRISE MEDICAL TO NOTIFY OF THESE TWO INCIDENTS. NO NEW INCIDENT TRANSPIRED AND NO SERIOUS INJURIES OCCURRED DURING EITHER OF THE TWO REPORTED INCIDENTS.
Patient problems: Fall; Head Injury
MAUDE report 12759583 ↗MalfunctionOct 19, 2021Misassembly by Users; Misassembly by Users
FATHER OF END USER WAS DESCENDING A RAMP AT THE DOCTOR'S OFFICE WHEN THE VOYAGE SEAT UNEXPECTEDLY SLID OFF THE BASE. THE CHILD FELL TO THE GROUND AND SUFFERED A HEAD INJURY REPORTED AS BRUISING. FOLLOW-UP MEDICAL EXAM INCLUDING HEAD CT SCAN DID NOT REVEAL ANY OTHER INJURIES.
Patient problems: Fall; Head Injury
MAUDE report 12657330 ↗InjurySep 24, 2021Misassembly by Users; Misassembly by Users
MOTHER REPORTED THAT SHE REMOVED VOYAGE FROM VEHICLE AND PLACED HER SON (END USER) IN THE STROLLER. SHE STATED THAT WHEN THEY WERE IN THE STORE AND TURNED THE CORNER THE SEAT DETACHED FROM THE BASE AND THE WHOLE SEAT FELL ON TOP OF THE END USER. AMBULANCE WAS CALLED. SHE STATED THAT END USER GOT A BLOODY NOSE AND A HEAD CONTUSION FROM THE IMPACT BUT NO OTHER INJURIES. MOTHER STATED THAT SHE THOUGHT THAT SHE DID NOT PLACE THE END USER CORRECTLY IN THE SEAT.
Patient problems: Fall; Head Injury
MAUDE report 12528987 ↗
Other Chair, With Casters devices
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- MEDLINE MDS808210ABEMedline Industries, Inc. · CHAIR, WITH CASTERS75 reports
- Ki TykeKi Mobility, LLC · Chair, With Casters1 recall0 reports
- MEDLINE MDS808200KDMedline Industries, Inc. · CHAIR, WITH CASTERS22 reports
- MEDLINE MDS808200ABEMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- Guardian MDS868BTRBMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- MEDLINE TCB228N21SMedline Industries, Inc. · CHAIR, WITH CASTERS6 reports
- GUARDIAN G1-503WCPX1Medline Industries, Inc. · CHAIR, WITH CASTERS5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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