device · product 1 of 1
Medtronic O-arm Imaging System Product Usage: image-intensified fluoroscopic x-ray system, mobile
- Recall number
- Z-0926-2013
- Initiated
- January 31, 2013
- Classification
- Class II
- Status
- Terminated
- Recalling firm
- Medtronic Navigation, Inc.
- Quantity
- 463 units
App-derived interpretation
Potential failure of the braking system that controls the O-arm Imaging System gantry movement in the vertical direction
Official device-enrichment evidence · Sourced
Component design/selection
Inspect official wording and provenance
Reason for recall
Potential failure of the braking system that controls the O-arm Imaging System gantry movement in the vertical direction
Code information
Product Catalog Numbers: 9732719, 9732719R, 9733346, 9733346R, BI-700-00027, BI-700-00027R, BI-700-00027-GER, BI-700-00027-GERR, BI-700-00027-100, BI-700-00027-100R, BI-700-00027-120, BI-700-00027-120R, BI-700-00027-230, BI-700-00027-230R Units with serial numbers 101 through 564 and unit 580 are affected. Serial numbers 565 and higher are not affected .
Distribution pattern
Worldwide Distribution - USA Nationwide and the countries of: Canada, AUSTRIA, BELGIUM, BRAZIL, BULGARIA, CHILE, CHINA, CROATIA, CZECH REPUBLIC, DENMARK,FINLAND, FRANCE, GERMANY, GREECE, INDIA, IRELAND, ISRAEL, ITALY, JAPAN ,KOREA, REPUBLIC OF KUWAIT, LEBANON, LIBYAN ARAB JAMAHIRIYA, MEXICO, NETHERLANDS, New Zealand, POLAND, RUSSIAN FEDERATION, SAUDI ARABIA, SINGAPORE, SLOVAKIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, Taiwan(R.O.C.) , THAILAND, TURKEY, UNITED ARAB EMIRATES. and UNITED KINGDOM.