MuscleMaster.com is recalling all lots and expiration dates of the seventeen below listed dietary supplements sold between June 1, 2009 and November 17, 2009. FDA informed MuscleMaster.com that it believes that the Recalled Products contain ingredients that are steroids. Specifically, FDA advised MuscleMaster.com of its concern that the Recalled … [Read more...]
McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products
Please see our post from yesterday regarding this OTC medication recall by McNeil Consumer Healthcare. … [Read more...]
ev3 Endovascular Inc. Trailblazer Support Catheter: Class I Recall
Product Name: Trailblazer Support Catheter Model Numbers SC-014-135, SC-018-090, SC-035-065, SC-035-135, SC-014-150, SC-018-150, SC-035-090, SC-035-150. Lot Numbers 7828282, 7792290, 7792584, 7805570, 7805797, 7806392, 7820252, 7790666, 7791887, 7803307, 7835331, 7822400, 7822593, 7800446, 7800555, 7800756, 7800779, 7800809, 7801822, 7801875, … [Read more...]
Nationwide Recall Of All Lots Of Tylenol Arthritis Pain 100 Count With Ez-Open Cap
McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is expanding its voluntary recall to include all available product lots of TYLENOL ® Arthritis Pain Caplet 100 count bottles, with the distinctive red EZ-OPEN CAP (Full list of lot numbers provided below). In November 2009, 5 lots of this product were recalled due to consumer reports of an … [Read more...]
Encompass Group Recalls Thermoflect Product Line
Jea R. Gackowski, Encompass Group Corporate Compliance Officer announced today the company is voluntarily recalling the Thermoflect product line for relabeling regarding its use in the MR (Magnetic Resonance) environment. "We are voluntarily recalling the product line from use in the Magnetic Resonance (MR) environment," Gackowski said. "We are … [Read more...]
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