Device recall
Z-1236-03: Critikon brand Adult, DURA-CUF, product code 2790, used as an arm cuff in…
FDA device recall · Class III · GE Medical Systems Information Technologies
Key facts
| Recall number (Z-number) | Z-1236-03 |
|---|---|
| Recall event | 26245 |
| Product | Critikon brand Adult, DURA-CUF, product code 2790, used as an arm cuff in association with a blood pressure monitor. |
| Recalling firm | GE Medical Systems Information Technologies |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 6, 2008 |
| 510(k) numbers | K974080 |
| FEI number | 1030184 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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