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Recall Observatory FDA recall evidence

Device product

Philips Healthcare Xper vascular systems R7.6 Model : 722134 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and thrombolysis and atherectomics), pacemaker Implantations and electrophysiology (EP). Use of the Allura Xper series system in the OR environment is restricted; the system should only be used for endo-vascular procedures. The Philips Integris Allura 9F is intended for diagnostic cardiovascular, vascular and interventional procedures

Z-0354-2016

February 03, 2015

Class II

Product summary

Firm
Philips Medical Systems, Inc.
Event
Event 70370
Status
Terminated
Classification
Class II
Quantity
22 units
Official record key
device-enforcement:Z-0354-2016

Official wording

Reason: Monitor Ceiling Suspension system may fall

Code information: S/N: 201 261 262 274 267 284 260 308 265 276 265 278 269 266 266 282 248 323 263 322 168 325

Distribution pattern: Worldwide Distribution - US Nationwide and the countries of: Canada,Australia, Austria, Brazil, Chile, China, Denmark, France, Germany, India, Italy, Japan, Mexico, Netherlands, South Africa, Spain, Switzerland and United Kingdom.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Monitor Ceiling Suspension system may fall