Tag: the Food and Drug Administration

FDA warns another drugmaker over tainted meds

You may have thought you were playing it safe by avoiding recently-recalled Johnson & Johnson products, but another drugmaker is now in the hot seat for some of the same problems, including the release of metal-tainted pills.
On Thursday, the U.S. Food and Drug Administration issued a warning letter to one of the world’s largest manufacturers of generic drugs, Michigan-based Perrigo Co.
The FDA said Perrigo failed to take appropriate action after the FDA cited the drug maker with a number of violations following an inspection of its facilities earlier in the year.
The first violation was issued for releasing products that didn’t meet quality control standards, including ibuprofen tablets contaminated with metal shavings from an equipment failure, the FDA said.
Read More: By Blake Ellis, CNNMoney.com

FDA docs: J&J knew of problems with Motrin in 2008

Johnson & Johnson learned of potential problems with its Motrin formula in 2008, but instead of issuing a recall, hired an outside contractor which began buying up the products, according to congressional investigators.

Colleen Goggins, J&J’s president for McNeil consumer products, will testify before House lawmakers Thursday about ongoing quality problems with its over-the-counter medications.

Last month McNeil recalled more than 40 varieties of children’s medicines after Food and Drug Administration inspectors discovered a slew of violations at a company plant.

Some of the medicines recalled contained tiny particles of metal, though federal health regulators say the risk of health risks is remote.

The recall is the latest in a series that threaten to tarnish J&J brands like Tylenol and Benadryl.

Lawmakers will question Goggins about the latest problems as well as its handling of a 2009 recall.

Read More: -By Matthew Perrone, the Associated Press


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