Device recall
Z-1496-04: Pacific Hemostasis brand SickleScreen Sickling Hemoglobin Screening Kit, Fisher…
FDA device recall · Class III · Fisher Diagnostic, A Company of Fisher Scientific LLC
Key facts
| Recall number (Z-number) | Z-1496-04 |
|---|---|
| Recall event | 30004 |
| Product | Pacific Hemostasis brand SickleScreen Sickling Hemoglobin Screening Kit, Fisher Diagnostics catalog number 100250, containing reagents for 30 determinations. |
| Product code | GHM |
| Recalling firm | Fisher Diagnostic, A Company of Fisher Scientific LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 3, 2005 |
| 510(k) numbers | K854079 |
| FEI number | 1181121 |
At a glance
- 1–9 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