Device recall
Z-0974-2018: CMI (Collagen Meniscus Implant) device, Ivy Sports Medicine s collagen-based…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-0974-2018 |
|---|---|
| Recall event | 79030 |
| Product | CMI (Collagen Meniscus Implant) device, Ivy Sports Medicine s collagen-based meniscus implant Product Usage: The CMI device, Ivy Sports Medicine s collagen-based meniscus implant, is comprised primarily of bovine type I collagen (nominally 99%) derived from tendon and small quantities of… |
| Product code | OLC |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2936485 |
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