Philips Medical Systems, Inc. recalls Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211
- Recall date
- January 23, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1251-2015
- FDA classification
- Class II
- Brand / firm
- Philips Medical Systems, Inc.
- Sold / distributed
- Worldwide Distribution. Argentina, Australia, Burkina-Faso, Chile, China, Colombia, Ecuador, France, Germany, Hungary, Indonesia, Iraq (NL), Kuwait, Libya, Macedonia, Malaysia, Mayotte, Poland, Saudi Arabia, Slovenia, Spain, Switzerland, Turkey, United Kingdom, and Uzbekistan.
Why it was recalled
Improper installation of Tube arm, and Wall stand may cause it to fall down, Improper installation of table may cause it to float.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211
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