Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1742-2022 — ZAP-X Radiosurgery System

U.S. FDA — Device Enforcement · United States · 2022-07-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1742-2022
Date of alert
2022-07-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zap Surgical Systems
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00860183001504
Reported risk: Software issue identified in cases of initial patient setup with large (greater-than-or-equal-to 1.5 degrees) rotational deviations, between digitally reconstructed radiographs, and pre-delivery X-ray images. In these cases the transitional alignment algorithm may incorrectly calculate the new treatment table offset values, leading to an incorrect position for the subsequent treatment isocenter.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.