Device recall
Z-1022-03: Catalog SBA11GLMMD, Sterile General Local Tray, Mfg date 5/20/03, exp date…
FDA device recall · Class II · Cardinal Health
Key facts
| Recall number (Z-number) | Z-1022-03 |
|---|---|
| Recall event | 26609 |
| Product | Catalog SBA11GLMMD, Sterile General Local Tray, Mfg date 5/20/03, exp date 1/01/05, order 101466; |
| Product code | LRO |
| Recalling firm | Cardinal Health |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 22, 2005 |
| FEI number | 3001236905 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database