Withdrawal of a medicinal preparation that does not comply with the specifications
The Ministry of Health and Prevention decided to withdraw the medicinal preparation "Core Daily 1-women Tablets", from the manufacturer "Country Life", due to its lack of conformity with the specifications.
The manufacturer demanded that it be withdrawn from the government and private sectors.
In a circular to health facilities and health care practitioners in the private sector, the Ministry confirmed that the results of the product analysis showed that it does not conform to the approved specifications when compared to the reference product.
She added that it is not registered in its drug administration, demanding that it not be dispensed and returned to the supplier.
She also asked any drug user to contact her in the event of side effects.
In a second circular, the Ministry decided to withdraw operations of the Telacomp ES-K medical device manufacturer Paul Hartmann AG.
They are gauze pads that contain x-ray detectable tangles.
It stated that the manufacturer had withdrawn operations due to complaints from clinics and suppliers that its X-ray strings were susceptible to breakage and abrasion upon mechanical stress.
The Ministry recommended health facilities to withdraw batches if they were found, indicating that the product is not registered in its drug administration.
In a third circular, the Ministry warned against the Medumat Standard “emergency and transport ventilator” due to the possibility that it will not operate.
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