Device recall
Z-1939-2010: Hospital Grade Power Cord, UL, Part # 66319, 055476, manufactured by…
FDA device recall · Class II · Medtronic Cardiovascular Revascularization & Surgical Therap
Key facts
| Recall number (Z-number) | Z-1939-2010 |
|---|---|
| Recall event | 55749 |
| Product | Hospital Grade Power Cord, UL, Part # 66319, 055476, manufactured by Electri-Cord Manufacturing Co. beginning in February 2003. The cords are a detachable unit, supplied with the instruments listed below: Medtronic Bio-Console 550 centrifugal pump console, Model #95180, Catalogue # 95180, E95180… |
| Product code | DWA |
| Recalling firm | Medtronic Cardiovascular Revascularization & Surgical Therap |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 24, 2011 |
| 510(k) numbers | K051303, K941921, K953118, K972894 |
| FEI number | 1000116158 |
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