Immulite 1000 CEA Catalog No. LKCE1
FDA device recall Z-0972-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Diagnostic Products Corp
- Reason for recall
- Instabililty
- Action taken
- Notice was made via email or telephone. Users are to discard kits.
- Root cause
- Other
- Status
- Terminated
- Product code
- DHX
- Quantity affected
- 884
- Date initiated
- 2004-05-03
- Date posted
- 2004-07-20
- Date terminated
- 2004-07-01
- Location
- Los Angeles, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| IMMULITE CEA (K970877) | Diagnostic Products Corp. | 1997-09-22 |