Device recall
Z-1917-2008: Celsus Laboratories Heparin Lithium Lyophilized; Lithium Heparin for use in…
FDA device recall · Class II · Celsus Laboratories Inc
Key facts
| Recall number (Z-number) | Z-1917-2008 |
|---|---|
| Recall event | 48084 |
| Product | Celsus Laboratories Heparin Lithium Lyophilized; Lithium Heparin for use in blood collection tube devices and in vitro diagnostic devices. |
| Product code | JKA |
| Recalling firm | Celsus Laboratories Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 21, 2012 |
| FEI number | 1527761 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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