Device recall
Z-0676-06: Gemcal Reference Serum (magnesium calibrator). Calibrator, Multianalyte Mixture…
FDA device recall · Class II · Alfa Wassermann, Inc
Key facts
| Recall number (Z-number) | Z-0676-06 |
|---|---|
| Recall event | 34687 |
| Product | Gemcal Reference Serum (magnesium calibrator). Calibrator, Multianalyte Mixture. Level 1 and Level 2 Chemistry Control. |
| Product code | JIX |
| Recalling firm | Alfa Wassermann, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 18, 2006 |
| 510(k) numbers | K930104 |
| FEI number | 1000122044 |
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