Device recall
Z-1104-2012: Presource Custom Sterile Surgical and Procedure Kits containing Ethicon Ethilon…
FDA device recall · Class II · Cardinal Health
Key facts
| Recall number (Z-number) | Z-1104-2012 |
|---|---|
| Recall event | 61048 |
| Product | Presource Custom Sterile Surgical and Procedure Kits containing Ethicon Ethilon Black Nylon Nonabsorbable Surgical Sutures in new Tyvek packaging; surgical trays; Cardinal Health. The kits are custom packed with all of the specific disposable class 1 and 2 devices required by the customer for… |
| Product code | LRO |
| Recalling firm | Cardinal Health |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 1, 2016 |
| 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