Doribax recall

March 5, 2014

The Medicines and Healthcare Products Regulatory Agency (MHRA) said Janssen-Cilag Ltd is recalling Doribax (doripenem) 500mg powder for solution for infusion. The recall was based on the company’s portfolio review and followed from the decision to return the licence to Shionogi & Co Ltd, MHRA said. There were no known quality of safety issues with the recall, it said.

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Pharmacy Daily | Doribax recall

Doribax recall

Other recent headlines

WA group stocks vapes

Fujitsu to protect against cyber threats

PD breaking news – Queensland pharmacies scope of practice pilot expanded

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES