device · product 1 of 1
Philips Medical System Allura Xper X-Ray Angiographic
- Recall number
- Z-1120-2015
- Initiated
- June 06, 2014
- Classification
- Class II
- Status
- Terminated
- Recalling firm
- Philips Medical Systems, Inc.
- Quantity
- 7439
App-derived interpretation
software error
Official device-enrichment evidence · Sourced
Radiation Control for Health and Safety Act
Inspect official wording and provenance
Reason for recall
In certain circumstances, a software error can lead to a situation where the five minute fluoroscopy audible signal does not sound.
Code information
Software releases: PBL 10, 20, 30, 40, 50, and 60; CV20; R7.2x; R7.6; R8.1; and R8.2.
Distribution pattern
Worldwide Distribution - USA nationwide including Puerto Rico, Austria, Azerbaijan, Australia, Algeria, Argentina, Albania, Brazil, Belgium, Bangladesh, Bahamas, Bulgaria, Cambodia, Chile, Canada, China, Croatia, Czech Republic, Netherlands, New Zealand, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Romania, Reunion, Singapore, Slovenia, South Africa, Spain, Sudan, Sweden, Saudi Arabia, Switzerland, Syria, Taiwan, Thailand, France, Dominican Republic, Colombia, Turkey, Germany, Greece, Hong Kong, Denmark, Ecuador, Egypt, Estonia, Finland, Vietnam, Russian Federation, Iran, Iraq, Ireland, Israel, Italy, India, Indonesia, Japan, Jordan, Kenya, South Korea, Kuwait, Latvia, Lebanon, Lithuania, Macedonia, Malaysia, Mauritius, Mexico, Moldavia, Mongolia, Morocco, Nepal, Ukraine, United Arab Emirates, and United Kingdom