Device recall
Z-0337-2014: Centricity Perinatal and Centricity Intensive Care is intended to be used in…
FDA device recall · Class II · GE Healthcare It
Key facts
| Recall number (Z-number) | Z-0337-2014 |
|---|---|
| Recall event | 64805 |
| Product | Centricity Perinatal and Centricity Intensive Care is intended to be used in clinical departments healthcare delivery systems such as a Labor and Delivery, Postpartum Maternal Care, newborn Nursery, critical care units including Neonatal Intensive Care Units (NICU), and may also be used in… |
| Product code | HGM |
| Recalling firm | GE Healthcare It |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 10, 2016 |
| 510(k) numbers | K111614 |
| FEI number | 3004526608 |
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