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Batch recall of pharmaceutical products

Publication date: 01/01/1994

Publication ref: 400/94/6600V

Urgent Medicine Recall. This refers to medicines for human use that are licensed medicinal products as defined in the Medicines Act 1968, and which are withdrawn or recalled from sale or supply for safety, quality or efficacy reasons.

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The Prescription Medicines Code of Practice Authority (PMCPA) is responsible for administering the ABPI Code of Practice for the Pharmaceutical Industry at arm's length of the ABPI itself.

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