LONDON (Reuters) - U.S. drugmaker Mylan
The Medicines and Healthcare products Regulatory Agency, or MHRA, said the decision was due to the potential for small particles of white material to be present in individual vials.
The Mylan recall is being made on behalf of Strides Arcolab International and relates to Agila-branded supplies, the MHRA added. The Pennsylvania-based company bought Agila, a unit of India's Strides Arcolab
The issue with the Agila antibiotic follows a series of quality problems affecting medicines manufactured in India that have tarnished the country's reputation as a supplier of cheap generic drugs.
(Reporting by Ben Hirschler, editing by David Evans)