Drugs circulars and withdrawal

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The Saudi Food and Drug Authority publishes recall actions in a searchable database to ensure that the public has access to information on therapeutic items that have been withdrawn from the local market.
Recall action is the term used to describe an action taken to resolve a problem with a product currently in use or available for use because of deficiencies in its quality, safety, or efficacy. A product or specific batches may be recalled, corrective action taken and distributed again, special usage instructions given, or particular risks warned about without the product being withdrawn.

Do not stop using the product unless an alert inform that . not every alert in this database requires you to stop use.
If you are concerned about your health or if you have experienced an adverse event with the product you may be using please seek advice from a health provider or your physician as soon as possible. Also you can report any product adverse events directly to the available reporting channels of Saudi Food and Drug Authority (call center 19999 – the electronic reporting portal “Saudi vigilance” )

Published before 2023, click here .

 

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Type product
Beneficiaries
Trade Name Product Type Recall Action Recall Action level Date Details
MIMPARA 30MG F.C. TABLETS & MIMPARA 60MG F.C. TABLETS Medicine Product Wholesale level Hospital level Display
BISOLOL 10 mg Tablet Medicine Product Wholesale level Wholesale level Display
Three pharmaceutical products manufactured by SACO MEDICAL Medicine Product Recall Hospital level Display
HISTOP TAB 4MG Medicine Product Recall Hospital level Display
LINZESS Medicine Product Recall Retail level Display
Rantac Medicine Product Recall Hospital level Display
CIPROMAX 750MG TAB Medicine Product Recall Retail level Display
BENZOYL PEROXIDE 5 GEL Medicine Product Recall Retail level Display
BD ChloraPrep Clear (1ML) Medicine Product Recall Hospital level Display


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