Device recall
Z-1023-03: Catalog SBA61MJSFH, Sterile Laparotomy Pack, Mfg date 5/21/03, order 101438;
FDA device recall · Class II · Cardinal Health
Key facts
| Recall number (Z-number) | Z-1023-03 |
|---|---|
| Recall event | 26609 |
| Product | Catalog SBA61MJSFH, Sterile Laparotomy Pack, Mfg date 5/21/03, order 101438; |
| 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