Wockhardt recalls 5 drugs in UK after regulatory strictures
19 Oct 2013
Drug maker Wockhardt on Thursday recalled five over-the-counter (OTC) medicines in the UK following the withdrawal of good manufacturing practices (GMP) certificate for its Chikalthana, Aurangabad, unit last week (See: Wockhardt gets another slap from UK drug regulator).
After this, the UKMHRA directed pharmacies, dispensing clinics and wholesalers to return five different prescription-only medicines manufactured by the pharmaceutical company.
Among the medicines recalled four are for pain relief and one for Type 2 diabetes.
The recall was not at the patents level. According to the drug regulator, the products were tested on importation and Qualified Person (QP) released and that there is no evidence of a risk to patient safety from products currently in the UK market.
''However, it is considered that the products have not been manufactured in line with GMP requirements. People do not need to return their medicines because there is no evidence that the medicines affected by the precautionary recall in the UK are defective. Therefore, it's important that people continue to take their medicines as prescribed,'' Gerald Heddell, MHRA's director of inspection, enforcement and standards said in a statement.
In a communication last week, UKMHRA had told Wockhardt that it was replacing its GMP certificate to the Chikalthana facility with a restricted GMP certificate, allowing it to manufacture only critical medicines.
The new certification permits continued manufacturing and quality control testing of ''critical'' products in situations where it has been agreed by the national competent authority or European Medicines Agency that there is no feasible alternative in the market concerned, Wockhardt had said last week.
Accordingly, 10 prescription-only medicines can continue to be made at the Chikalthana site and still be supplied to patients in the UK, UKMHRA said on Thursday.
''This is because due to concerns over the continuity of supply, the benefits to patients of continuing to take these medicines outweigh the risk from any quality concerns with the medicine,'' the UK regulator said.
The UKMHRA's restricted GMP certification was seen as marginally positive for Wockhardt in terms of revenue and stock performances.
During an inspection at Wockhardt's Chikalthana unit in July, the UKMHRA had identified manufacturing deficiencies, including poor record keeping relating to the manufacture and testing of the medicines made at the site, and inadequate validation and production controls for medicines.
Earlier in July, the UKMHRA had passed a similar stricture involving 16 medicines against Wockhardt's Waluj, Aurangabad site (British drug regulator recalls 16 Wockhardt drugs).
