Device recall
Z-0627-03: AFP Control Kit distributed under the following label: AxSYM and IMx, Abbott…
FDA device recall · Class II · Abbott Health Products, Inc.
Key facts
| Recall number (Z-number) | Z-0627-03 |
|---|---|
| Recall event | 25554 |
| Product | AFP Control Kit distributed under the following label: AxSYM and IMx, Abbott Laboratories USA, North Chicago, IL 60064 |
| Product code | JJE |
| Recalling firm | Abbott Health Products, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 2, 2004 |
| FEI number | 2623532 |
At a glance
- None 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