FDA Device recall Z-0005-2018
Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
- FDA Device
- Class II
- terminated
- Published 2017-10-11
On 2017-10-11 the FDA classified a Class II recall of Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR by Permobil Ab, citing there is a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0005-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-09-01 |
| Published | 2017-10-11 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Permobil Ab |
| Distribution | US |
Product
Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
Reason
There is a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base.
Identifiers
| code_info | a) C300 CORPUS II, Serial Numbers: DOMESTIC: 43407264 43502593 43505689 2535000080 2535000452 2535000453 25350…a) C300 CORPUS II, Serial Numbers: DOMESTIC: 43407264 43502593 43505689 2535000080 2535000452 2535000453 2535000717 2535001026 2535001168 2535001320 2535001707 2535001800 2535001950 2535002178 2535002183 2535002275 2535002281 2535002304 2535002628 2535002986 2535003299 2535003587 2535003669 2535003720 2535003741 2535003742 2535003743 2535003744 2535003745 2535003785 2535003786 2535003787 2535003790 2535003791 2535003792 2535003793 2535003837 2535003838 2535003839 2535003841 2535003844 2535003845 2535003846 2535003847 2535003848 2535003849 2535003850 2535003851 2535003852 2535003853 2535003854 2535003855 2535003856 2535003917 2535003918 2535003921 2535003922 2535003923 2535003924 2535003925 2535003926 2535003938 2535003939 2535003940 2535003941 2535003967 2535003968 2535003969 2535003971 2535003986 2535003987 2535003988 2535003989 2535003990 2535003999 2535004000 2535004001 2535004002 2535004003 2535004025 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0005-2018%22
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