Device recall
Z-1984-2011: VARIANT nbs Sickle Program Resin Update CD-ROM; Model Number:250-3020, included…
FDA device recall · Class III · Bio-Rad Laboratories Inc
Key facts
| Recall number (Z-number) | Z-1984-2011 |
|---|---|
| Recall event | 55910 |
| Product | VARIANT nbs Sickle Program Resin Update CD-ROM; Model Number:250-3020, included in 250-3000; Distributed and Manufactured by Bio-Rad Laboratories, Inc. The VARIANT nbs Sickle Cell Program is intended as a qualitative screen for the presence of hemoglobins F, A, S, D, C and E in eluates of neonatal… |
| Product code | GKA |
| Recalling firm | Bio-Rad Laboratories Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 8, 2011 |
| FEI number | 2915274 |
At a glance
- None Linked 510(k)s
- 1–9 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