Device recall
Z-2300-2016: Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Package 18…
FDA device recall · Class II · Ge Healthcare It
Key facts
| Recall number (Z-number) | Z-2300-2016 |
|---|---|
| Recall event | 64758 |
| Product | Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Package 18 Product Usage: is an image management system intended to be used by trained professionals, including but not limited to physicians, nurses and medical technicians. The system is used with general purpose computing… |
| Product code | LLZ |
| Recalling firm | Ge Healthcare It |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2017 |
| 510(k) numbers | K052618 |
| FEI number | 3004526608 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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