Permobil Inc FDA Recalls

2 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
M5 Corpus Power Wheelchair REF,120032Class IIJun 19, 2025This recall is being reported retroactively. Power Platform	This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic.	Class IIDevices	Jun 19, 2025
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3Class IIFeb 29, 2024This recall has been reported retroactively. The power wheel	This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to mainta	Class IIDevices	Feb 29, 2024