Device recall
Z-1209-03: VIDAS Chlamydia Assay (CHL) for In-Vitro Diagnostic Use Product Number: 30101
FDA device recall · Class I · bioMerieux
Key facts
| Recall number (Z-number) | Z-1209-03 |
|---|---|
| Recall event | 26945 |
| Product | VIDAS Chlamydia Assay (CHL) for In-Vitro Diagnostic Use Product Number: 30101 |
| Product code | LJC |
| Recalling firm | bioMerieux |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 17, 2005 |
| 510(k) numbers | K915884 |
| FEI number | 3002769706 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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