iVIEW DAB Detecion Kit. Catalog Number 760-091
FDA device recall Z-0928-03 · posted 2003-06-17 · Terminated
Recall details
- Recalling firm
- Ventana Medical Systems Inc
- Reason for recall
- Kit does not stain tissues properly.
- Action taken
- Recall notification was made by telephone on May 6 and 7, 2003. A faxed letter and response form followed.
- Root cause
- Other
- Status
- Terminated
- Product code
- KTO
- Quantity affected
- 409 kits
- Distribution
- Nationwide.
- Date initiated
- 2003-05-07
- Date posted
- 2003-06-17
- Date terminated
- 2004-05-03
- Location
- Tucson, AZ
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.