Fortunately, no one had to overdose or lose their life because of the missing warning label, this was a recall done on the companies accord. “This is a wholesale and retail level recall and is not being undertaken on the basis of adverse events,” J&J said on the website. “No action is required by consumers or health-care providers and consumers can continue to use the product.” Three different Tylenol products used flavoring agents that contain less than 1 percent alcohol, and the alcohol content was listed on the package rather than the front of the bottle, according to a statement on J&J’s website.
According to Bloomberg Business Week, "In April, more than 40 types of J&J’s children’s over-the- counter liquid medicines were recalled, forcing a suspension of production at a plant and reducing 2010 sales about $600 million, the New Brunswick, New Jersey-based company said in July. The U.S. House Oversight and Government Reform Committee has been investigating J&J’s handling of the April recall and a separate incident involving Motrin tablets".
Products include:
- Tylenol Daytime 8 oz. Citrus Burst
- Tylenol Severe 8 oz. Cool Burst
- Tylenol Nighttime 8 oz. Cool Burst
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