Port Washington, NY, United States
Medical Depot Inc. recalls
2 recalls recorded since 2018, most recently on 11 April 2025. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)1
Ongoing Class I Medical devices
- Recall started
- 11 April 2025
- Reason
- Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
- Distribution
- Worldwide distribution - US Nationwide and the countries of Albania, Austria, Bahrain, Belgium, Bosnia and Herzegovina, Bulgaria, Canada, China, Colombia, Croatia, Cyprus, Czech Republic, France, Germany, Great Britain, Greece, Hong Kong, Hungary, Iceland, ISRAEL, Italy, JAPAN, Kenya, Kuwait, Latvia
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1727-2025
- iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.
Ongoing Class II Medical devices
- Recall started
- 14 June 2024
- Reason
- The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
- Distribution
- Nationwide Foreign: Canada
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-2354-2024, Z-2355-2024
- Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily activities. Model: 791BL (Blue)
- Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily activities. Model: 791RD (Red)
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.