Z-0841-2020 Class II Terminated
FDA device recall Z-0841-2020 was initiated by Palodex Group Oy on January 7, 2020 and is designated Class II. Reason for recall: Slow degradation of plastic insulation used in the PSU DC plug of the DIGORA Optime, Scan eXam, Express, GXPS-500 systems may result in short circuiting which may cause heating and melting. The meltin… The recall status is terminated (terminated April 15, 2024). Affected quantity: 4,563 Total Globally (all products).
Recall Details
- Product Type
- Devices
- Report Date
- January 29, 2020
- Initiation Date
- January 7, 2020
- Termination Date
- April 15, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4,563 Total Globally (all products)
Product Description
Reason for Recall
Distribution Pattern
US: WI and PA OUS: ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, COSTA RICA, CZECH REPUBLIC, DENMARK, ECUADOR, FINLAND, FRANCE, GERMANY, GREECE, HUNGARY, INDIA, ISRAEL, ITALY, JAPAN, KOREA, REPUBLIC OF, KUWAIT, MALAYSIA, MALTA, NETHERLANDS, NEW ZEALAND, NORWAY, OMAN, PAKISTAN, POLAND, QATAR, ROMANIA, RUSSIAN FEDERATION, SAUDI ARABIA, SERBIA, SINGAPORE, SLOVENIA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, REPUBLIC OF CHINA, THAILAND, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM, VIETNAM