Recall Z-2639-2025
Zap Surgical Systems · initiated July 25, 2025
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
ZAP-X Radiosurgery System, Model: 300150
Codes / lots: UDI-DI: 00860183001504, Serial Numbers: ZUC17153, ZUC20156, ZUC20157, ZUC20159, ZUC21162, ZUC21164, ZUC22166, ZUC22169, ZUC22170, ZUC22171, ZUC22173, ZUC22174, ZUC23176, ZUC23177, ZUC24179, ZUC24180, ZUC24181. Software version: TDS V1.10.1
Reason for recall
If the radiosurgery system triggers a proximity error message during a long gantry move (greater-than180 degrees), and a subsequent proximity error message occurs after the automatic reduction of speed, a software defect could potentially lead the collimator to collide with patient shoulders or the patient table.
FDA-determined cause: Software change control
Action taken
On 7/25/2025, correction notices were sent to customers who were asked to do the following: Firm will be revising the software to address this issue. Until we supply you with the revised software, the firm strongly advises that you follow these steps to prevent potential collisions. 1. In the rare event that the system triggers a proximity error message during a long gantry move (greater-than-180-degrees), and a subsequent proximity error message occurs after the automatic reduction of speed, please manually extract the patient. 2. After the patient has been safely extracted, please return the gantry to its home position before resuming any treatment procedures. If you have any further questions related to this situation email Derek@zapsurgical.com
Details
- Recall number
- Z-2639-2025
- Initiated
- July 25, 2025
- Posted by FDA
- September 26, 2025
- Product code
- IYE – Accelerator, Linear, Medical
- Quantity
- 17
- Distribution
- Worldwide - US Nationwide distribution in the states of FL, CO, NJ, NY and the countries of Germany, France, Spain, Poland, Republic of Korea, T¿rkiye, Paraguay.
- Recalling firm
- Zap Surgical Systems, San Carlos, CA