Device recall
Z-1336-04: Pacific Hemostasis D-Dimer Assay Kit, Fisher Diagnostics Catalog Number 100660…
FDA device recall · Class III · Fisher Diagnostic, A Company of Fisher Scientific LLC
Key facts
| Recall number (Z-number) | Z-1336-04 |
|---|---|
| Recall event | 29573 |
| Product | Pacific Hemostasis D-Dimer Assay Kit, Fisher Diagnostics Catalog Number 100660, packaged in a cardboard box containing materials and reagents to perform 80 tests. |
| Product code | GHH |
| Recalling firm | Fisher Diagnostic, A Company of Fisher Scientific LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 7, 2004 |
| FEI number | 1181121 |
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