Device recall
Z-2431-2015: Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit: Part number…
FDA device recall · Class III · Cepheid
Key facts
| Recall number (Z-number) | Z-2431-2015 |
|---|---|
| Recall event | 71841 |
| Product | Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit: Part number CT/NGSWAB-50; Microbiology: The Cepheid X pert CT /NG Vagina Endocervical/ Specimen Collection Kit is designed to collect, preserve and transport patient Chlamydia trachomatis and Neisseria gonorrhoeae DNA in endocervical and… |
| 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