Ventana Medical Systems Inc 2022-07-20 Health serious FDA
Health · FDA · Recall #FDA-Z-1374-2022
Ventana HE 600 System, automated slide preparer, for use in laboratories. Recall
Issued July 20, 2022 · Ventana Medical Systems Inc
In July 2022, Ventana Medical Systems Inc recalled the Ventana HE 600 System, automated slide preparer, for use in laboratories., a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
There is a potential for fluid leak inside the Ventana HE 600 instrument which could result in electrical short and fire
What you should do
- 1 Stop using Ventana HE 600 System, automated slide preparer, for use in laboratories. right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Ventana Medical Systems Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Ventana Medical Systems Inc
- Category
- Health
- Recall date
- July 20, 2022
- Units affected
- Not reported
- Sold at
- 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,
- Recall number
- FDA-Z-1374-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Ventana Medical Systems Inc has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.