Device recall
Z-0550-2007: Clark Biocompatible Hemoperfusion Cartridge, Sorbent: Heparinized polymer over…
FDA device recall · Class II · Clark Research and Development Inc
Key facts
| Recall number (Z-number) | Z-0550-2007 |
|---|---|
| Recall event | 37289 |
| Product | Clark Biocompatible Hemoperfusion Cartridge, Sorbent: Heparinized polymer over acitivated carbon, 50mL, Clark Research and Development, Inc. Folsom, LA 70437 |
| Product code | FLD |
| Recalling firm | Clark Research and Development Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 17, 2007 |
| FEI number | 2316506 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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