Medical DevicesNationwide
Ventana Medical Systems Inc iVIEW DAB Detecion Kit. Catalog Number 760-091 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
iVIEW DAB Detecion Kit. Catalog Number 760-091
Brand
Ventana Medical Systems Inc
Lot Codes / Batch Numbers
Lot 400566
Products Sold
Lot 400566
Ventana Medical Systems Inc is recalling iVIEW DAB Detecion Kit. Catalog Number 760-091 due to Kit does not stain tissues properly.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Kit does not stain tissues properly.
Recommended Action
Per FDA guidance
Recall notification was made by telephone on May 6 and 7, 2003. A faxed letter and response form followed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026