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in a searchable database to ensure that the public has access to information on therapeutic items that have been withdrawn from the local market.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and distributed again, special usage instructions given, or particular risks warned about without the product being withdrawn.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
Glutol Medicine Product Recall Hospital level Display
Celestone Chronodose Injection Ampoule Medicine Product Recall Wholesale level Display
DIPROFOS INJ. 2ML Medicine Product Recall Hospital level Display
VERTIZIN 75mg Capsule Medicine Product Recall Retail level Display
All pharmaceutical products manufactured by Verve Humancare Laboratories Medicine Product Recall Retail level Display
SODIUM ACETATE 20ML Medicine Product Recall Hospital level Display
MAGNESIUM OXIDE 400mg Tablet Medicine Product Recall Retail level Display
Twinzol Eye Drops Medicine Product Recall Retail level Display


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