Five months ago (in January 2010), McNeil Consumer Healthcare, a division of Johnson and Johnson, recalled millions of Tylenol and Motrin products stemming from complaints of an "unusual moldy, musty or mildew-like odor. Four times over the last seven months, McNeil has had to recall products. A variety of McNeil products have been included in the recalls: Tylenol, Zyrtec, Motrin, Benadryl as well as its children's line of non-prescription drugs.
On June 5, 2010, McNeil announced it was expanding the original January recall because some products were "inadvertently ommitted from the initial recall." UNBELIEVABLE! The drugmaker has now added four additional lots of Benadryl allergy ultratab tablets (100 count), and one product lot of extra strength Tylenol rapid release gels (50 count) to the recall.
McNeil's string of recalls has garnered a great deal of attention from the FDA. According to the FDA compliance office, the FDA has "serious concerns about the company's control over the quality of its drugs and the company's failure to aggressively investigate and correct quality problems." The case has been referred to the crime division, and criminal prosecution is a possibility.
On June 5, 2010, McNeil announced it was expanding the original January recall because some products were "inadvertently ommitted from the initial recall." UNBELIEVABLE! The drugmaker has now added four additional lots of Benadryl allergy ultratab tablets (100 count), and one product lot of extra strength Tylenol rapid release gels (50 count) to the recall.
McNeil's string of recalls has garnered a great deal of attention from the FDA. According to the FDA compliance office, the FDA has "serious concerns about the company's control over the quality of its drugs and the company's failure to aggressively investigate and correct quality problems." The case has been referred to the crime division, and criminal prosecution is a possibility.
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