Curing a headache shouldn’t be a headache. That’s why there’s new Tylenol Cheesesteak Rapid Release pain-relievers. It’s a delicious Philly Cheesesteak whose savory juices have been doused in the Paracetamol you love, but without the hassle. Plus a cheesesteak! [More]
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More Moldy Barfy Benadryl And Tylenol Recalled
By 6.17.10
Oopsy-poopsies! Johnson and Johnson forgot to recall four “lots” of Benadryl Allergy Ultratabs and one lot of Extra Strength Tylenol Rapid Release Gels along with the dozens already recalled in Jan. J&J took the pills off the market after consumers complained they smelled moldy and in a few cases, caused vomiting and diarrhea. [More]
Johnson & Johnson Hired Fake Shoppers To Buy Up Bad Motrin, Avoid Public Recall
By 6.14.10
Ever since the FDA and Congress started asking Johnson & Johnson to explain why it keeps recalling medicine, there have been references to an unpublicized “recall” that happened in November 2008. Last month, at a hearing of the House Oversight and Government Reform Committee, a J&J executive swore that the company didn’t mean to mislead anyone. It turns out that wasn’t exactly accurate: Bloomberg has obtained emails from J&J’s company, McNeil Consumer Healthcare, that show executives knew the secret recall would trigger an FDA reaction if the agency got wind of its full scope. [More]
PediaCare Pulled From Stores, Victim Of Latest Tylenol Recall
By 6.1.10
Blacksmith Brands bought the PediaCare line of children’s cough and cold medicines from Johnson & Johnson last November. Unfortunately, the company hadn’t switched production over to a different facility, so last Friday it had to recall nearly 100,000 bottles that are guilty by association. There have been no complaints so far about the products, but when your manufacturer is under investigation by the FDA’s criminal division you tend to want to play it safe. [More]
Tylenol Recall Factory Was Staffed With Undertrained Temps
By 5.31.10
The manufacturing plant that has been the cause of Johnson & Johnson’s latest in a string of recalls has already been described as dirty and poorly maintained. It turns out that it was also staffed with temps and contract employees who weren’t properly trained, according to tax records and an FDA inspection report filed earlier this year. [More]
Criminal Charges Are Possible For Tylenol Recall Scandal
By 5.27.10
CNN is reporting that the FDA has referred the Tylenol recall case to their criminal division for investigation. At issue is a pattern of non-compliance with FDA warnings and failures by management of McNeil to investigate and provide a timely resolution to serious problems with the product. These problems include excess amounts of the active ingredient in Tylenol, acetaminophen. [More]
FDA Announces Widespread Investigation Of McNeil After Tylenol Recalls
By 5.19.10
Remember the recalled liquid Tylenol and other children’s medicines last month? Or the stinky drugs that were recalled back in January? Or the children’s Tylenol that was recalled last September? The FDA remembers, which is probably why it’s “conducting a company-wide investigation of McNeil Consumer Healthcare’s drug manufacturing practices to determine whether similar problems exist throughout the company.” Also, a date has now been set (May 27) for the House Committee hearing where the CEO and chairman of parent company Johnson & Johnson are expected to testify. [More]
Congress Opens Investigation Into Children's Tylenol Recall
By 5.6.10
The House Committee on Oversight and Government Reform — the same crew behind the Toyota recall hearings — has announced that it has opened an investigation into the recent recall of Children’s Tylenol and several other brands of kids’ medicine. [More]
FDA: McNeil Plant That Made Recalled Tylenol Is A Dirty Stinkpot With No Quality Control
By 5.5.10
One of the implied promises of a brand name, especially when it comes to drugs, is you can expect higher quality, but maybe that doesn’t apply when it comes to McNeil products.The FDA says the plant that produced the recently recalled children’s Tylenol, Motrin, Zyrtec and Benadryl, was using raw materials that were contaminated with bacteria. The plant also lacked adequate quality-control procedures and was dirty. So far none of the recalled medicine has tested positive for bacterial contamination, but the FDA report suggests that the contaminated material was used to make the recalled lots. The plant has been shut down indefinitely. [More]
Children's Tylenol, Motrin, Other Medications Recalled
By 5.1.10
Head to your medicine cupboards and start checking out the children’s meds you might have there — the Food and Drug Administration announced today Johnson & Johnson’s McNeil Consumer Healthcare Unit has begun a voluntary recall of various medicines because of manufacturing discrepancies. [More]
FDA Is Mad: Funky, Smelly, Barfy Tylenol Has Been A Problem Since 2008
By 1.15.10
The FDA is @#$%# pissed off at McNeil, the company that makes smelly, barfy Tylenol and other products, because apparently this problem has been going on since 2008. [More]
Tylenol Recall Now Includes A Bunch Of Other Products
By 1.15.10
Some batches of a certain type of Tylenol had an unusual moldy, musty, or mildew-like odor that is associated with non-serious nausea, stomach pain, vomiting, or diarrhea. The smell is apparently from a chemical that was on the wood pallets the pills were stored on. Originally, the recall was just for one type of Tylenol. Now there is a big ass list, which includes some types of Motrin, Rolaids and St. Joseph brand products. [More]
Girl "Grows Back Face" After Pain Relief Pill Made It Turn Black And Fall Off
By 1.13.10
19-year old Eva Uhlin has regrown her face, chest, arms, back and stomach. A rare reaction to a couple pills of pain reliever acetaminophen, the main ingredient in Tylenol, caused her to develop Toxic Epidermal Necrolysis, and large parts of her skin turned black and fell off. [More]
DNA And Fingerprints Collected From 1982 Tylenol Poisoning Suspect
By 1.9.10
The 1982 Tylenol poisoning murders, the chief reason why the tamper-proof packages of modern over-the-counter medications must be broken into with, at minimum, a chainsaw, are being investigated again in light of new tips and new forensic techniques. Well, that only took 28 years. [More]
"Moldy Smelling" Tylenol Recalled
By 12.29.09
All TYLENOL® Arthritis Pain Caplet 100 count bottles with the distinctive red EZ-OPEN caps have been recalled after consumer complaints of “an unusual moldy, musty, or mildew-like odor that was associated with nausea, stomach pain, vomiting and diarrhea.” [More]
Tylenol Voluntarily Recalls Children's Medicines
By 9.25.09
Concerned about bacterial contamination, Tylenol is recalling certain children’s liquid medication products manufactured during a certain period in 2008. While the risk of infection is low when the medicines are ingested, still: eww, bacteria.
FDA May Take Vicodin And Percocet Off The Market
By 7.1.09
Bad news for Dr. Greg House and other, non-fictional chronic pain patients. The FDA advisory panel that met yesterday about the effects of excessive doses of acetaminophen made another recommendation to the FDA—to take popular painkillers Vicodin and Percocet (and their generic versions) off the market because of the effect both drugs can have on the liver when taken for extended periods. The FDA will most likely follow this recommendation.
FDA: Hey America, Stop Overdosing On Painkillers!
By 6.30.09
Look, we know this recession is tough and all, but you’ve gotta lay off the NyQuil and Theraflu or the FDA will stuff them behind a counter, ok? Seriously, an advisory panel is meeting today, and already voted to reduce the maximum daily dose of Tylenol and other painkillers. They might even slap scary “black box” warnings on all over-the-counter painkillers to dissuade you acetaminophen addicts from overdosing.
