Device recall
Z-1698-2023: Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808…
FDA device recall · Class II · C.R. Bard Inc
Key facts
| Recall number (Z-number) | Z-1698-2023 |
|---|---|
| Recall event | 92082 |
| Product | Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814, e) REF 51816, f) REF 51818 |
| 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