Device recall
Z-1075-2013: G7 HPLC. Used as an aid in the detection and presumptive identification of…
FDA device recall · Class III · Tosoh Bioscience Inc
Key facts
| Recall number (Z-number) | Z-1075-2013 |
|---|---|
| Recall event | 56584 |
| Product | G7 HPLC. Used as an aid in the detection and presumptive identification of abnormal hemoglobins in whole blood. |
| Product code | JPD |
| Recalling firm | Tosoh Bioscience Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 13, 2014 |
| 510(k) numbers | K011434, K020489 |
| FEI number | 3005529799 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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