Device recall
Z-1129-03: IMx Rubella IgM Reagent Kit, 100 tests, list 7A24-20; Abbott Laboratories…
FDA device recall · Class III · Abbott Laboratories HPD/ADD/GPRD
Key facts
| Recall number (Z-number) | Z-1129-03 |
|---|---|
| Recall event | 26868 |
| Product | IMx Rubella IgM Reagent Kit, 100 tests, list 7A24-20; Abbott Laboratories, Abbott Park, IL 60064 |
| Product code | LFX |
| Recalling firm | Abbott Laboratories HPD/ADD/GPRD |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 16, 2003 |
| 510(k) numbers | K931059 |
| FEI number | 1415939 |
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