Medical Depot Inc.: Device Recall

Recall #Z-1727-2025 · 04/11/2025

Class I: Dangerous

Recall Details

Recall Number: Z-1727-2025
Classification: Class I
Product Type: Device
Recalling Firm: Medical Depot Inc.
Status: Ongoing
Date Initiated: 04/11/2025
Location: Port Washington, NY, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 89,532 units

Reason for Recall

Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.

Product Description

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.

Distribution Pattern

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, Libya, Lithuania, Malaysia, Maldives, Nepal, Netherlands, Norway, Oman, Philippines, Poland, Portugal, Qatar, Romania, Russia, Saudi Arabia, Serbia, Slovak Republic, Slovenia, South Korea, Spain, Sri Lanka, Sweden, Switzerland, Taiwan, Thailand, Trinidad & Tobago, Turkey, Uganda, Ukraine, United Arab Emirates.

Other Recalls by Medical Depot Inc.

Class II: Risk 06/14/2024

The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
Class II: Risk 06/14/2024

The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury

View all recalls by Medical Depot Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.