Device recall
Z-3212-2018: Medtronic Clip Gun Magazines are packaged in individually sealed pouches and…
FDA device recall · Class II · Medtronic Neurosurgery
Key facts
| Recall number (Z-number) | Z-3212-2018 |
|---|---|
| Recall event | 80657 |
| Product | Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5 individually pouched Clip Gun Magazine. REF CM8902, Medtronic Clip Gun Magazine, Rx only, CE 0344, STERILE EO, Rx only, Single Use |
| Product code | HBO |
| Recalling firm | Medtronic Neurosurgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 30, 2022 |
| 510(k) numbers | K050044 |
| FEI number | 3015531529 |
At a glance
- 1–9 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