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

Recall Z-1825-2026 — Philips Spectral CT on Rails. Model Number: 728334.

U.S. FDA — Device Enforcement · United States · 2026-03-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1825-2026
Date of alert
2026-03-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
PHILIPS MEDICAL SYSTEMS
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00884838103627
Reported risk: Philips has identified three software issues: 1. During a continuous CT (CCT) scan, there is the potential that the Gantry could remain at the current scan position after pressing Go. 2. Potential where the message of Previous Surview Exists Select Previous Surview? <Yes> or <No> should display but does not appear. 3. After performing Surview and planning the Brain Helical acquisition by setting Brain Area DoseRight Index to increase the dose, there is the potential that the Define Head Area option in the context menu is grayed out.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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