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Philips Healthcare Inc. recalls Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single Detector, Dual Detector, Release 3) System
Recalled October 3, 2012 · FDA recall Z-2465-2012 · Philips Healthcare
Hazard
The Wireless Portable Detector (WPD) is not fixed securely inside the Mobile Detector Holder and may fall down · FDA Class II
Units
93 Units
Sold at
Worldwide Distribution--USA (nationwide) and the countries of Australia, Austria, Canada, Chile, Finland, France, Germany, Hungary. Italy, Japan, Latvia, Netherlands, New Zealand. Oman, South Korea, Switzerland and United Kingdom.
Description
The Wireless Portable Detector (WPD) is not fixed securely inside the Mobile Detector Holder and may fall down
Product
Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single Detector, Dual Detector, Release 3) System codes: 712020, 712022, 712025 This system is used for making X-ray exposures for diagnostics.
Manufacturer(s)
Philips Healthcare Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →