Device recall
Z-1442-2010: Instruction for Use for Symphony Double Pumping Kit; Medela, Inc., P.O. Box 660…
FDA device recall · Class II · Medela Inc
Key facts
| Recall number (Z-number) | Z-1442-2010 |
|---|---|
| Recall event | 54995 |
| Product | Instruction for Use for Symphony Double Pumping Kit; Medela, Inc., P.O. Box 660, 1101 Corporate Drive, McHenry, IL 60051-0660; the instructions were packaged with the following non-sterile single user accessory kits for use with Symphony breast pumps: a) Model 67023, Harmony to Symphony Conversion… |
| Product code | HGX |
| Recalling firm | Medela Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 10, 2010 |
| 510(k) numbers | K020518 |
| FEI number | 1419937 |
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