Device recall
Z-0228-2007: VerifyNow P2Y12 Assay Device Kit, Part Number 85054
FDA device recall · Class II · Accumetrics Inc
Key facts
| Recall number (Z-number) | Z-0228-2007 |
|---|---|
| Recall event | 36707 |
| Product | VerifyNow P2Y12 Assay Device Kit, Part Number 85054 |
| Product code | JOZ |
| Recalling firm | Accumetrics Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 26, 2012 |
| 510(k) numbers | K051231 |
| FEI number | 3001376288 |
At a glance
- 1–9 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