Device recall
Z-2943-2018: Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product…
FDA device recall · Class II · Bard Medical Division
Key facts
| Recall number (Z-number) | Z-2943-2018 |
|---|---|
| Recall event | 80624 |
| Product | Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads are packed into each urine collection kit carton along with a pre-connected drainage funnel, specimen container, funnel lid, specimen lid and a room label. |
| Product code | FMH |
| Recalling firm | Bard Medical Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 2, 2020 |
| FEI number | 1018233 |
At a glance
- None 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