Device recall
Z-2432-2015: Xpert CT/NG Urine Specimen Collection Kit Part number GXCT/NGURINE-50…
FDA device recall · Class III · Cepheid
Key facts
| Recall number (Z-number) | Z-2432-2015 |
|---|---|
| Recall event | 71841 |
| Product | Xpert CT/NG Urine Specimen Collection Kit Part number GXCT/NGURINE-50; Microbiology: Xpert CT/NG Urine Specimen Collection Kit is designed to preserve and transport Chlamydia trachomatis and Neisseria gonorrhoeae DNA in first-catch male and female urine specimens from symptomatic and asymptomatic… |
| Product code | LSL |
| Recalling firm | Cepheid |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 28, 2015 |
| 510(k) numbers | K121710 |
| FEI number | 3004530258 |
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