Device recall
Z-2326-2015: S4C Occiput Torque Wrench F/Set Screw; used to tighten the S4 Cervical Spinal…
FDA device recall · Class II · Aesculap, Inc.
Key facts
| Recall number (Z-number) | Z-2326-2015 |
|---|---|
| Recall event | 71709 |
| Product | S4C Occiput Torque Wrench F/Set Screw; used to tighten the S4 Cervical Spinal System clamping screws with a defined torque 2.8 Nm for tightening the clamping screw in the screw head/hook head/occipital plate/transverse connector and other connectors. |
| Product code | HXC |
| Recalling firm | Aesculap, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2017 |
| 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