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McNeil Consumer Healthcare Recall [Drug]
Sep 6, 2013 Out of an abundance of caution, McNeil is voluntarily recalling the three lots released to the market made with the same batch of active
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Establishment Inspection Report
Procedure defines the requirements for assessing any potential product recall promptly and for implementing recall activities at McNeil Healthcare LLC, Las
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McNeil, a Johnson Johnson Subsidiary FDA Case Study
by W Adis 2014 Cited by 2 McNeil faced other recalls and QA problems during this timeframe. It also had to recall Zyrtec, Motrin, Benadryl and adult Tylenol.
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