| Subject: | FDA Announces Class I Recall Of Two Unapproved Devices |
| Category: | Food and Drug Administration (FDA)
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| Published: | Tue, 16 Dec 2008 - 12:00 pm |
| The U.S. Food and Drug Administration (FDA) has announced a Class 1 Recall for two unapproved and un-cleared devices whose manufacturers claim they can treat various medical conditions. A Class 1 Recall means that there is a reasonable probability that the use of a device will cause adverse health consequences or death. The manufacturers, VIBE Technologies of Greeley, Colo., and Nebion LLC of Los Angeles, Calif., claimed their devices treated conditions ranging from cancer to migraines. The FDA... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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