Device recall
Z-3117-2026: Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray…
FDA device recall · Class II · C.R. Bard Inc
Key facts
| Recall number (Z-number) | Z-3117-2026 |
|---|---|
| Recall event | 98840 |
| Product | Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF: INTP16 INTS14 INTS14C INTS16 INTS16C PEDINTS06 PEDINTS08 PEDINTS10 UDI code: 00801741183300 10801741183307 00801741183218 10801741183215 00801741183232 10801741183239 00801741183225 10801741183222 00801741183249… |
| Product code | KOD |
| Recalling firm | C.R. Bard Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K000723 |
| FEI number | 1018233 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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