Ki TykeRecalls & reported problems
Ki Mobility, LLC · Tyke for x:panda Size 1 · Class 1
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Nov 19, 2021Terminated
The Instructions for Use provided with the device contained information intended for use of a mechanical wheelchair, not a chair with casters.
Z-0467-2022 · Root cause: Process design · FDA record ↗
Other Chair, With Casters devices
- MEDLINE MDS808210AREMedline Industries, Inc. · CHAIR, WITH CASTERS115 reports
- MEDLINE MDS808210ABEMedline Industries, Inc. · CHAIR, WITH CASTERS75 reports
- Zippie Voyage Voyage; Voyage VIPSunrise Medical (US) LLC · Chair, With Casters1 recall9 reports
- MEDLINE MDS808200KDMedline Industries, Inc. · CHAIR, WITH CASTERS22 reports
- Guardian MDS868BTRBMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- MEDLINE MDS808200ABEMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- MEDLINE TCB228N21SMedline Industries, Inc. · CHAIR, WITH CASTERS6 reports
- SARA STEDY NTB2000Arjohuntleigh AB · Chair, With Casters5 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.