Device recall
Z-0120-2008: AmniSure ROM Test, Fetal Membrane Rupture Test for In-Vitro Diagnostic Use…
FDA device recall · Class II · AmniSure International LLC
Key facts
| Recall number (Z-number) | Z-0120-2008 |
|---|---|
| Recall event | 44937 |
| Product | AmniSure ROM Test, Fetal Membrane Rupture Test for In-Vitro Diagnostic Use, Model: FMRT-1, AmniSure International LLC, Cambridge, MA 02138 |
| Product code | JJX |
| Recalling firm | AmniSure International LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 6, 2008 |
| 510(k) numbers | K030849 |
| FEI number | 3005345832 |
At a glance
- 1–9 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