| Subject: | FDA Issues Class I Recall For The Nebion HLX-8 Magnetic Resonance Device |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 6 Oct 2008 - 02:00 pm |
| The Food and Drug Administration (FDA) has issued a Class I Recall for the Nebion HLX-8 Magnetic Resonance Device. This product was manufactured from December 25, 2006 through June 11, 2008, and distributed from June 1, 2007 through June 11, 2008. The company's labeling reported that the device could be used to treat many different medical conditions and diseases such as: Cancer (including breast, bone, lung, and pancreatic)Carpel tunnel syndrome Migraines Premenstrual syndrome... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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