Device recall
Z-1308-2025: Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf…
FDA device recall · Class II · Aesculap Inc
Key facts
| Recall number (Z-number) | Z-1308-2025 |
|---|---|
| Recall event | 96223 |
| Product | Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf Hysterectomy Forceps STR 210MM; (2) REF BJ501R, Phaneuf Hysterectomy Forceps ANG 205MM; (3) REF BJ511R, Holzbach Hyst Forceps CVD245MM; (4) REF BJ520R, Heaney Hyst Forceps Grooved 205MM; (5) REF BJ521R, Heaney Hyst Forceps… |
| Product code | HGC |
| Recalling firm | Aesculap Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2916714 |
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