RecallDepth

Azurion IGTS Fixed Systems

Company
Philips North America
Recall Initiated
October 4, 2023
Posted
September 30, 2024
Recall Number
Z-0229-2024
Firm Location
Cambridge, MA

Reason for Recall

Philips has become aware of an issue with the Philips Integris-Allura, Allura Xper and Azurion systems that have been delivered to Puerto Rico without a warning label and the Source-to-Skin Distance Spacer (Tube-spacer) is missing.

Distribution

United States Territories of Puerto Rico, Guam, and Virgin Islands

Lot / Code Info

Azurion 7 M12 465 Azurion 7 M20 702 Azurion 7 M20 942 Azurion 7 M20 948 Azurion 7 M20 503

Root Cause

Device Design

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