Device recall
Z-1013-2010: Bio-Rad VARIANT II Hemoglobin A1c Program Recorder Pack with Calibrator/Diluent…
FDA device recall · Class III · Bio-Rad Laboratories Inc
Key facts
| Recall number (Z-number) | Z-1013-2010 |
|---|---|
| Recall event | 52719 |
| Product | Bio-Rad VARIANT II Hemoglobin A1c Program Recorder Pack with Calibrator/Diluent Set, Model Number 270-2101NU Manufactured by Bio-Rad Laboratories, Hercules, CA |
| Product code | LCP |
| Recalling firm | Bio-Rad Laboratories Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 2, 2011 |
| 510(k) numbers | K070452 |
| FEI number | 2915274 |
At a glance
- 1–9 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