Device recall
Z-0011-04: Power cord manufactured by ElectriCord Manufacturing Company, P/N 316579, used…
FDA device recall · Class II · GE Medical Systems Information Technologies
Key facts
| Recall number (Z-number) | Z-0011-04 |
|---|---|
| Recall event | 26293 |
| Product | Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAMAP Patient Monitors as Follows: DINAMAP PRO Series, DINAMAP PRO 1000 Monitor under both the Critikon and GE Medical Systems. The company name EliectriCord is on the power cord plug. |
| Product code | MWI |
| Recalling firm | GE Medical Systems Information Technologies |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 2012 |
| 510(k) numbers | K012915, K020022, K021435 |
| FEI number | 1030184 |
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