Device recall
Z-3114-2026: Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray…
FDA device recall · Class II · C.R. Bard Inc
Key facts
| Recall number (Z-number) | Z-3114-2026 |
|---|---|
| Recall event | 98840 |
| Product | Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes: 00801741024801 10801741024808 00801741024818 10801741024815 00801741024825 10801741024822 SureStep" Foley Tray System with Bardex Lubricath Temp Sensing Foley Catheter REF: A119416M… |
| Product code | EZC |
| Recalling firm | C.R. Bard Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K910197, K910846 |
| FEI number | 1018233 |
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