Device recall
Z-0866-2024: MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm)…
FDA device recall · Class II · Aesculap Inc
Key facts
| Recall number (Z-number) | Z-0866-2024 |
|---|---|
| Recall event | 93793 |
| Product | MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL HLD STR JAW 220MM"; |
| Product code | HCF |
| 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