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Warning Date
    2017-08-22

SFDA Withdraws "Jusprin 81mg Product" duo to Quality Defects

2017-08-22


SFDA has withdrawn "Jusprin 81mg Product", produced by Gulf Pharmaceutical Industries (Julphar) duo to quality defects. The Authority has addressed the health authorities to stop using the product.

This action took a place after manufacturer reported, a quality issue in the products, to SFDA.SFDA has forced Julphar Company to withdraw all batches from all facilities dispensing the drug. The Authority called on the consumers of this product to consult the specialist doctor.

For further information, please contact SFDA call center (19999).

Drugs
  • To report sector-related issues

  • Call Centre 19999


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