Device recall
Z-1311-2025: Numerous models of nonsterile hemostatic forceps: (1) REF FB458R, Glover…
FDA device recall · Class II · Aesculap Inc
Key facts
| Recall number (Z-number) | Z-1311-2025 |
|---|---|
| Recall event | 96223 |
| Product | Numerous models of nonsterile hemostatic forceps: (1) REF FB458R, Glover ATR.CLAMP CVD 215MM; (2) REF FB459R, Glover ATR.CLAMP CVD 245MM; (3) REF FB461R, Glover ATR.CLAMP 195MM; (4) REF FB462R, Glover ATR.CLAMP 210MM; (5) REF FB469R, Leland-Jones Peripheral CLMPSTR 195MM; (6) REF FB567R, Cooley… |
| Product code | HXD |
| 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
- 1–9 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