FDA issues most serious recall for certain speed control dials used for wheelchairs

Nov 25, 2025 - 02:20 PM
FDA-device-recall

The Food and Drug Administration has identified a Class I recall of Max Mobility/Permobil SpeedControl Dials used with the SmartDrive MX2+ Power Assist Device for wheelchairs after identifying a design issue that can lead to unexpected behavior of the SmartDrive motor. The FDA said Max Mobility/Permobil reported two serious injuries associated with the issue.

In addition, the FDA issued an early alert for certain Fresenius Kabi Ivenix LVP Primary Administration Sets due to an assembly defect.

Related News Articles

Headline
FDA issues recall, alerts for certain convenience kits; companies voluntarily recall certain IV fluids
The Food and Drug Administration has identified a Class I recall of certain convenience kits by AVID Medical that contain recalled Medline Namic Angiographic…
Headline
FDA issues early alerts for multiple products 
The Food and Drug Administration has issued early alerts for the following products: •    Certain epidural kits by Medical Action…
Headline
Highest FDA recall issued for certain convenience kits by Medline 
The Food and Drug Administration has identified a Class I recall of certain Medline convenience kits containing B. Braun components that have Huons Bupivacaine…
Headline
Highest FDA recall issued for certain convenience kits
The Food and Drug Administration Aug. 3 identified Class I recalls of two convenience kit products. Certain kits by Medline…
Headline
FDA announces highest recall for certain ventilators, introducer kits
The Food and Drug Administration has identified Class I recalls of two products: certain Astral ventilators by Resmed due to a supercapacitor that may leak…
Headline
Baxter recalls certain IV bags due to possible particulate matter 
Baxter is voluntarily recalling a specific lot of intravenous solution due to a report of particulate matter in the solution identified as cardboard, according…