Device recall
Z-0542-05: RAPID SYPHILIS TEST KIT, per insert, contents of the kit are: 1 Rapid Syphilis…
FDA device recall · Class II · Ups Supply Chain Solutions
Key facts
| Recall number (Z-number) | Z-0542-05 |
|---|---|
| Recall event | 31097 |
| Product | RAPID SYPHILIS TEST KIT, per insert, contents of the kit are: 1 Rapid Syphilis test cassette, 1 alcohol swab, 1 buffer container, 1 lancet (needle), 1 zipped bag, 1 pipette (plastic) (included with cassette). There is no firm identified on the product packaging. |
| Recalling firm | Ups Supply Chain Solutions |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 27, 2005 |
| FEI number | 3004071323 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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