Device recall
Z-1882-2011: iSite PACS with iSite ViewForum Applications, R7.4V6 L1 L2, L3, Versions…
FDA device recall · Class II · Philips Medical Systems
Key facts
| Recall number (Z-number) | Z-1882-2011 |
|---|---|
| Recall event | 58044 |
| Product | iSite PACS with iSite ViewForum Applications, R7.4V6 L1 L2, L3, Versions: 3.6.96, 3.6.101, 3.6.110, 4.1.96, 4.1.101, and 4.1.110 ; Product is manufactured and distributed by Philips Medical Systems, Foster City, CA ViewForum Applications: iSite ViewForum Applications is an image processing… |
| Product code | LLC |
| Recalling firm | Philips Medical Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 18, 2011 |
| 510(k) numbers | K032096 |
| FEI number | 3002971142 |
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