Device recall
Z-1323-2022: EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated…
FDA device recall · Class II · DePuy Spine, Inc.
Key facts
| Recall number (Z-number) | Z-1323-2022 |
|---|---|
| Recall event | 90390 |
| Product | EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients with cervical disc disease (DDD). Part Number: CUI8060L |
| Product code | MAX |
| Recalling firm | DePuy Spine, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K170503 |
| FEI number | 1526439 |
At a glance
- 1–9 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