Philips North America recalls Zenition 50 & 70 Mobile Surgery C-arm
Recalled Product
Zenition 50 & 70 Mobile Surgery C-arm
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: Zenition 50 974 Zenition 50 1244 Zenition 50 1247 Zenition 50 892 Zenition 70 1735 Zenition 70 1824
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