Drug recall
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
FDA recall event 99075 · Class II · Accuray Incorporated
Key facts
| Event ID | 99075 |
|---|---|
| Recall numbers | Z-2640-2026 |
| Recalling firm | Accuray Incorporated |
| Product type | Devices |
| Products | Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using… |
| Initiation date | Jun 16, 2026 |
| Report date | Jul 8, 2026 |
| City | Madison |
| State | WI |
| Country | United States |
| FEI number | 3003873069 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: