Device recall
Z-0500-2022: ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing and…
FDA device recall · Class II · Konica Minolta Healthcare Americas, Inc.
Key facts
| Recall number (Z-number) | Z-0500-2022 |
|---|---|
| Recall event | 89275 |
| Product | ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing and presentation of medical images on display monitors for medical diagnostics Product number: ADFR and ADJC |
| Product code | LLZ |
| Recalling firm | Konica Minolta Healthcare Americas, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 5, 2024 |
| 510(k) numbers | K210066 |
| FEI number | 2241281 |
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