RockHard Laboratories announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplement sold under the name RockHard Weekend (RHW) specific to the following Lot Numbers: Blister Pack: T12 705 08 (exp: 10/11) / T12 705 09 (exp: 3/12, 8/12) 3ct Bottle: R417 0509 (exp: 09/12) 8ct Bottle: T237-0509 (exp: … [Read more...]
Cardiovascular Systems Recalls ViperSheath Sheath Introducer
Cardiovascular Systems, Inc. has announced a voluntary recall of all lots of the ViperSheathTMSheath Introducer on behalf of Thomas Medical due to reports about stretching or fracture of the sheath during use. CSI initiated the nationwide recall on November 2, 2009. The ViperSheathTM Sheath Introducer is a product developed and manufactured by … [Read more...]
Cardiac Science Notifies AED Customers of Nationwide Voluntary Medical Device Correction
Cardiac Science Corporation is initiating a voluntary field correction after it was determined certain automated external defibrillators (AEDs) may experience a rare product issue in which the AED may not be able to deliver therapy during a resuscitation attempt. Device failure may affect resuscitation of the patient, which could lead to serious … [Read more...]
IDS Sports Conducts a Voluntary Nationwide Recall of Bromodrol, Dual Action Grow Tabs, Grow Tabs, Mass Tabs, and Ripped Tabs TR
IDS Sports announced today that it is conducting a voluntary nationwide recall of five of the company’s dietary supplement products sold under the following names: Bromodrol, Dual Action Grow Tabs, Grow Tabs, Mass Tabs, and Ripped Tabs TR. The Food And Drug Administration (FDA) has notified IDS Sports that the recalled products contain the … [Read more...]
GMP Herbal Products Recalls Weight Loss Supplement Found to Contain Undeclared Drug Ingredients
GMP Herbal Products, Inc. has been informed by the Food and Drug Administration (FDA) that Pai You Guo, a weight loss dietary supplement, sold and marketed by the firm contains undeclared drug ingredients. FDA lab analyses of dietary supplements distributed by the company were found to contain undeclared sibutramine, an FDA-approved drug used as … [Read more...]
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