Device recall
Z-1720-2016: Accriva- APTT Cuvette for use on the Hemochron Jr. test system, catalog #J103…
FDA device recall · Class II · Accriva Diagnostics Inc., dba ITC, dba Accumetrics
Key facts
| Recall number (Z-number) | Z-1720-2016 |
|---|---|
| Recall event | 73949 |
| Product | Accriva- APTT Cuvette for use on the Hemochron Jr. test system, catalog #J103, lot B6JCA012. |
| Product code | JPA |
| Recalling firm | Accriva Diagnostics Inc., dba ITC, dba Accumetrics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 14, 2016 |
| 510(k) numbers | K940401 |
| FEI number | 2250033 |
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