Device recall
Z-0289-2008: A1CNOW+ with sampler 10-Test Kits (Product No: 3022), Metrika, Inc., Sunnyvale…
FDA device recall · Class II · Metrika Inc
Key facts
| Recall number (Z-number) | Z-0289-2008 |
|---|---|
| Recall event | 44752 |
| Product | A1CNOW+ with sampler 10-Test Kits (Product No: 3022), Metrika, Inc., Sunnyvale, CA 94085. (This test provides quantitative measurement of the percent of glycated hemoglobin (%A1C) levels in capillary (fingerstick) or venous whole blood samples. The test is used by professional healthcare providers… |
| Product code | LCP |
| Recalling firm | Metrika Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 25, 2008 |
| 510(k) numbers | K051321 |
| FEI number | 3002940409 |
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