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
Check against the official notice below — it lists the full affected range.
Permobil, Ab is recalling 5,539 electric wheelchairs sold nationwide and in multiple countries including Australia, Canada, and several European nations. The affected models are the C300 CORPUS II, C350 CORPUS II, C400 CORPUS II, C400 CORPUS II LR, C500 CORPUS II, and C500 CORPUS II LR. The recall addresses a potential failure of the top plate assembly, which is the component connecting the seating system to the wheelchair base.
The recall includes specific serial numbers for the affected wheelchairs. The source document does not specify what action affected consumers should take in response to this recall.
Written by software from the official notice below. Not reviewed by a lawyer.
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.
Reason for recall: 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. Distribution: Nationwide and Australia, Benelux, Canada, Denmark, Finland, France, Germany, Israel, Norway, Sweden, and UAE Quantity: 5539 units Lot/code info: 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 2535004026 2535004027 2535004079 2535004080 2535004081 2535004082 2535004085 2535004086 2535004087 2535004088 2535004089 2535004090 2535004091 2535004092 2535004093 2535004094 2535004095 2535004129 2535004140 2535004142 2535004143 2535004157 2535004158 2535004159 2535004174 2535004175 2535004176 2535004177 2535004178 2535004179 2535004180 2535004181 2535004182 2535004183 2535004184 2535004210 2535004211 2535004212 2535004213 2535004214 2535004263 2535004264 2535004265 2535004266 2535004267 2535004268 2535004321 2535004322 2535004323 2535004324 2535004325 2535004326 253500432
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.