3D Ceiling Suspension
FDA device recall Z-0987-03 · posted 2003-07-10 · Terminated
Recall details
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Reason for recall
- the back up safety catch may not function properly
- Action taken
- Letters dated 4/15/03 and 4/23/03 were issued to the accounts along with instructions on how to fix the problem.
- Root cause
- Other
- Status
- Terminated
- Product code
- IZF
- Quantity affected
- 3504 units
- Distribution
- The product was shipped nationwide to medical facilities.
- Date initiated
- 2003-04-15
- Date posted
- 2003-07-10
- Date terminated
- 2005-04-11
- Location
- Malvern, PA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| MULTIX U. BUCKY TABLE X-RAY UNIT (K803130) | Siemens Corp. | 1981-01-28 |
| MULTIGRAPH (K790765) | Siemens Corp. | 1979-04-26 |