device · product 1 of 1
Ventana HE 600 System, automated slide preparer, for use in laboratories.
- Recall number
- Z-1374-2022
- Initiated
- June 01, 2022
- Classification
- Class II
- Status
- Ongoing
- Recalling firm
- Ventana Medical Systems Inc
- Quantity
- 763 instruments
App-derived interpretation
There is a potential for fluid leak inside the Ventana HE 600 instrument which could result in electrical short and fire
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Inspect official wording and provenance
Reason for recall
There is a potential for fluid leak inside the Ventana HE 600 instrument which could result in electrical short and fire
Code information
All Lots; UDI/DI: 04015630976010
Distribution pattern
US: AL AR AZ CA CO CT DC FL GA HI IA IL IN KS KY MA MD MI MN MO MS MT NC NE NJ NY OH OK OR PA PR SC SD TN TX UT VA WA WI WV OUS: Canada, Austria, Belgium, Croatia, Denmark, Finland, France, Germany, Greece, Ireland, Italy, Luxembourg, Netherlands, Norway, Poland, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey, UK, Argentina, Australia, Brazil, Chile, China, Colombia, Costa Rica, Ecuador, Egypt, El Salvador, Guatemala, Hong Kong, Israel, Japan, Kuwait, Lebanon, Malaysia, Saudi Arabia, Singapore, South Korea, Taiwan, Thailand, United Arab Emirates (UAE), Vietnam