MX 16-Slice CT Scanner System. Used as a whole-body computed tomography X-Ray system.
Reported: October 23, 2013 Initiated: July 22, 2013 #Z-0019-2014
Product Description
MX 16-Slice CT Scanner System. Used as a whole-body computed tomography X-Ray system.
Reason for Recall
A pinch point at the end of the table top can cause injury.
Details
- Recalling Firm
- Philips Medical Systems (Cleveland) Inc
- Units Affected
- 326
- Distribution
- Worldwide Distribution-USA including the states of AL, AR, CA, FL, GA, IL, IN, KY, MS, NC, NJ, NV, NY, OH, PA, and VA; and countries of: Albania, Algeria, Argentina, Australia, Austria, Belgium, Bolivia, Brazil, Cambodia, China, Ghana, Greece, India, Indonesia, Ireland, Italy, Jordan, Latvia, Lebanon, Libya, Lithuania, Malawi, Mexico, Nepal, Netherlands, Oman, Palestine, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Switzerland, Thailand, Turkey, Uganda, Ukraine, Uzbekistan, Venezuela and Vietnam.
- Location
- Cleveland, OH
Frequently Asked Questions
What product was recalled? ▼
MX 16-Slice CT Scanner System. Used as a whole-body computed tomography X-Ray system.. Recalled by Philips Medical Systems (Cleveland) Inc. Units affected: 326.
Why was this product recalled? ▼
A pinch point at the end of the table top can cause injury.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 23, 2013. Severity: Moderate. Recall number: Z-0019-2014.
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