Drugs circulars and withdrawal
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in a searchable database to ensure that the public has access to information on therapeutic items that have been withdrawn from the local market.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and distributed again, special usage instructions given, or particular risks warned about without the product being withdrawn.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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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 |