Permobil Electric Wheelchair Bases Recalled for Top Plate Assembly Failure
Permobil is recalling 146 electric wheelchair bases due to a potential failure of the top plate assembly that connects the seating system to the base.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a structural component of a mobility device that could fail, posing a risk of harm to the user, but the source text does not report any specific injuries or illnesses.
Plain-English summary
Permobil, Ab is recalling 146 units of electric wheelchair bases, including models C300, C350, C400, and C500. The recall is due to a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base.
The affected units were distributed nationwide in the United States as well as in Australia, Benelux, Canada, Denmark, Finland, France, Germany, Israel, Norway, Sweden, and the UAE. Specific serial numbers for the affected units are listed in the agency's recall record.
Consumers should stop using the affected wheelchair bases and contact Permobil, Ab for further instructions on the recall.
The recalled product
- Product
- Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
- Manufacturer
- Permobil, Ab
- Category
- Medical Device — Mobility Aids
- Hazard
- Affected units
- 146
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- a) C300
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Permobil, Ab under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same manufacturer · Permobil, Ab
See all →- HighPermobil Recalls Powered Wheelchairs Due to Backrest Bar Failure Risk
FDA (Devices) · 2018-09-26
- HighPermobil Recalls Electric Wheelchairs Due to Top Plate Assembly Failure Risk
FDA (Devices) · 2017-10-11
Same hazard · structural failure
See all →- SevereMondraker Recalls Mountain Bicycles with ONOFF S9 Carbon Handlebars
CPSC · 2026-09-03
- HighFord F-650 SD Recall: Liftgate Platform Deck Pins May Break
NHTSA · 2026-08-20
- HighStryker Hoffmann II Connecting Rod Micro May Crack After Cleaning and Sterilization
FDA (Devices) · 2026-08-05
- HighStryker Hoffmann II Connecting Rod Micro May Crack After Cleaning and Sterilization
FDA (Devices) · 2026-08-05
- High