FDAFDA · Food and drugs·Recall number Z-0766-2016
Philips Healthcare TraumaDiagnost; Codes: 72001, 720011, 720013, 720020; A radiological examination unit for emergency work and routine skeletal diagnosis.
Published February 17, 2016 · Recall initiated: July 22, 2015
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
If arm is not fastened securely it could fall down.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Philips Electronics North America Corporation
- Distributor
- Distributed in the states of NY, WI, MA, AL, FL, GA, RI, CA, KS, and TX, and the countries of Canada, Australia, Austria, Belgium, France, Germany, Ireland, Italy, Netherlands, New Zealand, Portugal, South Africa, Spain, and Switzerland.
- Lot
- All TraumaDiagnost products that were delivered before the week of July 2, 2007.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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