Digital Fluorographic System model DFP-2000A.
FDA device recall Z-0100-04 · posted 2003-11-06 · Terminated
Recall details
- Recalling firm
- Toshiba American Med Sys Inc
- Reason for recall
- Images display with wrong patient demographics.
- Action taken
- Firm has issued to it''s service persons orders to install a software fix on 27 May 2003.
- Root cause
- Other
- Status
- Terminated
- Product code
- JAA
- Quantity affected
- 471
- Distribution
- Naitonwide.
- Date initiated
- 2003-05-27
- Date posted
- 2003-11-06
- Date terminated
- 2005-03-15
- Location
- Tustin, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| TDA-4000/A4 (K941611) | Toshiba America Medical Systems, In.C | 1994-05-13 |