Johnson & Johnson's latest recall was caused by a typo that inserted the bête noire of high-school English teachers -- a double negative -- into dosing instructions on more than 667,000 Sudafed ...

McNeil Consumer Healthcare is recalling, at the wholesale level in the U.S., nine product lots of Sudafed 24-hour, pseudoephedrine HCl, extended-release tablets.

Sudafed PE is different from regular Sudafed. ... You should read the product labels carefully for all of the drugs that you take. This is because several over-the-counter ...

Phenylephrine products, such as Sudafed PE, are available without a prescription and are found on retailers' shelves, including at grocery stores and drugstores.

Yet another recall for the Johnson & Johnson tally. This time, we're back to consumer drugs. McNeil Consumer Healthcare is pulling nine lots of Sudafed tablets--667,632 packages, to be ...

Johnson & Johnson is dealing with another recall – this time, the recall is due to a typo on 667,000 Sudafed packages.. McNeil Consumer Healthcare recalled the decongestant because the dosing label ...