Philips North America recalls Veradius Unity Mobile Surgery C-arm
Recalled Product
Veradius Unity 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: Veradius Neo 497 Veradius Neo 607 Veradius Neo 619
View official government recall
Were you affected by this recall?
If you were harmed by a recalled product, you may have legal options. Consider speaking with a consumer protection lawyer in your state.
Looking for safe alternatives?
Browse certified-safe products in this category on Amazon →
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime