Device recall
Z-1200-2013: Presource PBDS, Shoulder Arthroscopy, Kit, Circulator
FDA device recall · Class I · Cardinal Health, Medical Products & Services
Key facts
| Recall number (Z-number) | Z-1200-2013 |
|---|---|
| Recall event | 64736 |
| Product | Presource PBDS, Shoulder Arthroscopy, Kit, Circulator |
| Product code | OFP |
| Recalling firm | Cardinal Health, Medical Products & Services |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 12, 2017 |
| FEI number | 3001236905 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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