Permobil recalls

Permobil has 4 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 5 Aug 2026. 4 are still ongoing. 2 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls4since 2023

Last 12 months2reported

Class I00% of total

Ongoing4latest 5 Aug 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 2 0

Severity split

Class I 0 0%Class II 4 100%Class III 0 0%

Why permobil is recalled

Product types

Wheelchairs, Beds & Lifts250%
Other Medical Devices250%

By year

2026250%
2023250%

Ongoing permobil recalls

4 active

Reported	Class	Recall	Company	Reason	Where
5 Aug 2026Device	CLASS II	M5 Corpus Power Wheelchair recalled by Permobil	Permobil	Other	Nationwide
5 Aug 2026Device	CLASS II	M3 Corpus Power Wheelchair with Heavy Duty Shock recalled by Permobil	Permobil	Potency & Assay	Nationwide
5 Jul 2023Device	CLASS II	PushTracker E3 component utilized recalled by Permobil	Permobil	Device Malfunction	TN
5 Jul 2023Device	CLASS II	PushTracker E2 component utilized recalled by Permobil	Permobil	Device Malfunction	TN

All permobil recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
5 Aug 2026Device	CLASS II	M5 Corpus Power Wheelchair recalled by Permobil	Permobil	Other	Nationwide
5 Aug 2026Device	CLASS II	M3 Corpus Power Wheelchair with Heavy Duty Shock recalled by Permobil	Permobil	Potency & Assay	Nationwide
5 Jul 2023Device	CLASS II	PushTracker E3 component utilized recalled by Permobil	Permobil	Device Malfunction	TN
5 Jul 2023Device	CLASS II	PushTracker E2 component utilized recalled by Permobil	Permobil	Device Malfunction	TN

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.