Device recall
Z-1239-03: MDA Simplastin L, Product number 252555, 10 vials, 40 ml ea (400 test each)…
FDA device recall · Class III · bioMerieux
Key facts
| Recall number (Z-number) | Z-1239-03 |
|---|---|
| Recall event | 27008 |
| Product | MDA Simplastin L, Product number 252555, 10 vials, 40 ml ea (400 test each), bioMerieux Inc., Box 15969 Durham, North Carolina 27704-0969. |
| Product code | GJS |
| Recalling firm | bioMerieux |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 18, 2004 |
| FEI number | 3002769706 |
At a glance
- None 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