Device recall
Z-1224-2011: Pump in Style Advanced (PNSA)Breast Pump; a daily use, double pump, electric…
FDA device recall · Class III · Medela Inc
Key facts
| Recall number (Z-number) | Z-1224-2011 |
|---|---|
| Recall event | 57597 |
| Product | Pump in Style Advanced (PNSA)Breast Pump; a daily use, double pump, electric powered breast pump; Manufactured exclusively by and for Medela, Inc., P.O. Box 660, 1101 Corporate Drive, McHenry, IL 60051-0660; the affected breast pumps were sold in the following configurations: a) article 57027 - Kit… |
| Product code | HGX |
| Recalling firm | Medela Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 21, 2012 |
| 510(k) numbers | K031614 |
| 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