Device recall
Z-2200-2008: Intran Plus, Disposable Intrauterine Pressure Catheter System, Part numbers…
FDA device recall · Class II · Utah Medical Products, Inc
Key facts
| Recall number (Z-number) | Z-2200-2008 |
|---|---|
| Recall event | 48679 |
| Product | Intran Plus, Disposable Intrauterine Pressure Catheter System, Part numbers IUP-400, IUP-400S, IUP-450, IUP-450S, IUP-500, IUP-550, IUP-600, IUP-600S, IUP-650, IUP-650S, IUP-700, IUP-750, Sterile, Single Use, Utah Medical Products Inc., 7043 South 300 West, Midvale, Utah 84047. |
| Product code | HFN |
| Recalling firm | Utah Medical Products, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 23, 2011 |
| 510(k) numbers | K905563, K955443, K961424 |
| FEI number | 1718873 |
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