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Lupin recalls birth control pills from US market

The product was manufactured at the company's facility in Pithampur, Madhya Pradesh

By PTI in New Delhi

  • Published 7.04.19, 11:42 AM
  • Updated 7.04.19, 11:42 AM
According to the US Food and Drug Administration, it is a voluntary nationwide recall due to a situation in which use of the product may cause temporary or medically reversible adverse health consequences
According to the US Food and Drug Administration, it is a voluntary nationwide recall due to a situation in which use of the product may cause temporary or medically reversible adverse health consequences (Shutterstock)

Drug firm Lupin is recalling more than 12,000 cartons of Fayosim tablets, used to prevent pregnancy, from the American market, as per a report of the US health regulator.

The reason for recall is "Failed impurities/degradation specifications: out-of-specification results observed in related substance test in Ethinyl Estradiol tablets USP 0.01mg at 12 month long term stability study," the Enforcement Report of the United States Food and Drug Administration (USFDA) said.

Lupin Pharmaceuticals Inc is recalling 12,464 cartons of the Fayosim (levonorgestrel and ethinyl estradiol) tablets USP, (0.15 mg/0.02 mg, 0.15 mg/0.025 mg, 0.15 mg/0.03 mg) and ethinyl estradiol tablets USP (0.01 mg) packaged in 1 extended-cycle wallet of 91 tablets packed in a pouch, it added.

The product was manufactured by Lupin Ltd at its Pithampur facility in Madhya Pradesh.

The voluntary ongoing nationwide recall is a class II recall, the report by the regulator said.

As per the USFDA, a class II recall is initiated in a "situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote."

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