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

Recall Z-1791-2025 — Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;

U.S. FDA — Device Enforcement · United States · 2025-05-13 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1791-2025
Date of alert: 2025-05-13
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Philips North America Llc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00884838099746

Reported risk: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

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-1791-2025 — Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;

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