Device recall
Z-1701-2023: HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b)…
FDA device recall · Class II · C.R. Bard Inc
Key facts
| Recall number (Z-number) | Z-1701-2023 |
|---|---|
| Recall event | 92082 |
| Product | HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF 71818 |
| Product code | EZD |
| Recalling firm | C.R. Bard Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K150345 |
| 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