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Drug Recall Probe Goes Nationwide

The Food and Drug Administration, or FDA, said Monday it is expanding nationwide its investigation of a Johnson & Johnson unit linked to the recall of some 50 children’s versions of Tylenol, Motrin, Benadryl and other defective drugs. On May 6, five days after the recall, the FDA issued a report identifying 20 violations at […]


Recalled Drugs Contaminated By Bacteria, FDA Says

Some of the 40 varieties of children’s cold medicines recalled by Johnson & Johnson last week were contaminated with bacteria, according to the Food and Drug Administration, or FDA. The FDA report, posted online, lists more than 20 manufacturing problems found at the Pennsylvania plant where the products were made. The recalled products include children’s […]


Infusion Pump Recalled After FDA Toughens Rules

This blog has run many posts about the dangers that defective medical devices present to the general public. On April 28 we reported that the Food and Drug Administration, or FDA, was issuing preliminary rules toughening the rules for approving the commercial sale of infusion pumps. Now there is a new development: the main U.S. […]

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