Philips North America recalls Integris-Allura IGTS Fixed Systems
Recalled Product
Integris-Allura IGTS Fixed Systems
Hazard / Issue
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.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: INTEGRIS Allura 15-12 (mono) 68
View official government recall
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