Home / Recalls / Medical Depot Inc. / Z-1727-2025

Z-1727-2025 Class I Ongoing

Recalled by Medical Depot Inc. — Port Washington, NY

FDA device recall Z-1727-2025 was initiated by Medical Depot Inc. on April 11, 2025 and is designated Class I. Reason for recall: Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing. The recall status is ongoing. Affected quantity: 89,532 units.

Recall Details

Product Type
Devices
Report Date
May 21, 2025
Initiation Date
April 11, 2025
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
89,532 units

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.

Reason for Recall

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

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.

Code Information

DC Cord Code Info: Catalog No. DV6X-619; UDI 885304020585; Cord Revision: Rev E; Lot No. beginning with 2023-01-01 through 2024-12-31. iGo2 Portable Oxygen Concentrator Systems Code Info: Catalog No. 125D, 125D-XB, 125D-BT, 125D-BT-XB, 125D-ARYA-XB; UDI 885304022237, 885304032250, 885304033257, 885304033240, 885304033516; Lot No. D23125001DS to D23A26121DS, D23706001DA to D23B16056DA, F23B06001DS to F25108143DS, F23313001DH to F25109259DH, F24212001DA to F25217150DA.

Other recalls by Medical Depot Inc.

  • Z-2354-2024 Class II — Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the (June 14, 2024)
  • Z-2355-2024 Class II — Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the (June 14, 2024)
  • Z-2103-2016 Class II — Universal aluminum crutch, 1 pair per case Aid the user in walking while reli (February 17, 2016)
  • Z-2105-2016 Class II — Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 (February 17, 2016)
  • Z-2101-2016 Class II — Aluminum crutch under the following labels: 1) Aluminum crutch, adult, 1 pair pe (February 17, 2016)
  • Z-2102-2016 Class II — EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crut (February 17, 2016)
  • Z-2104-2016 Class II — Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 (February 17, 2016)
  • Z-2106-2016 Class II — Direct Supply aluminum crutch, adult, 1 pair per case Aid the user in walking (February 17, 2016)

FDA data resources