Device recall
Z-0726-2023: Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215
FDA device recall · Class II · Corin Ltd
Key facts
| Recall number (Z-number) | Z-0726-2023 |
|---|---|
| Recall event | 91183 |
| Product | Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215 |
| Product code | LZO |
| Recalling firm | Corin Ltd |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3002806725 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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