Device recall
Z-0663-2010: AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in…
FDA device recall · Class II · KCI USA, Inc.
Key facts
| Recall number (Z-number) | Z-0663-2010 |
|---|---|
| Recall event | 53802 |
| Product | AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cord #4102204 used with Tricell 60601 Model 212857, First Step Select Model 215200 , and Plexipulse Model 205835. |
| Product code | IOQ |
| Recalling firm | KCI USA, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 21, 2011 |
| 510(k) numbers | K944567 |
| FEI number | 1625774 |
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