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

Recall Z-0466-2026 — Radiography 7300 C; Model Number: 712037;

U.S. FDA — Device Enforcement · Germany · 2025-10-01 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0466-2026
Date of alert: 2025-10-01
Country / jurisdiction: Germany
Risk level: Class II
Risk type: recall
Brand: Philips Medical Systems DMC GmbH
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00884838116016

Reported risk: Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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.

Recall Z-0466-2026 — Radiography 7300 C; Model Number: 712037;

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