Enalapril 10mg Arya

Enalapril 10mg Arya

Company name & Address: Registration number Batch number(s) Expiry date Pack size First release date Re-call Classification Recall date
Arya Pharma Pty Ltd

Pharma HQ, Corner Barbara and North Reef Road,

Elandsfontein,

Germiston,

Gauteng,

1601.

 

37/7.1.3/0328

 

GQQ24066
GQQ24064
GQQ24067
GQQ24053

 

 

GQQ24066 (Sep-2026)
GQQ24064 (Sep-2026)
GQQ24067 (Sep-2026)
GQQ24053 (Aug-2026)

 

 

28’s

 

GQQ24066 (Jan-2025)

GQQ24064 (Jan-2025)

GQQ24067 (July-2025)

GQQ24053 (Jan-2025)

 

Class II Type A

 

29 July 2026

 

Brief description of the problem (reason for recall)

Quality defect: This recall is initiated due to out-of-specification results observed during post-marketing surveillance studies.

Advice for health professionals and distributors:

Arya kindly request that you immediately refrain from selling or distributing the affected batches listed above. Additionally, please inform your patients to return any affected stock to your dispensary. Please quarantine all remaining stock and return it to your supplying warehouse or distributor with immediate effect. Arya Pharma Pty Ltd will arrange for the collection of all returned stock, and appropriate credit will be issued. Kindly retain this recall letter in a prominent location for one month, as additional stock may still be in transit.

 

For further product information, please call Arya Pharma Pty Ltd on 010 060 0740/4.

 

Proposed action taken and its urgency: A SAHPRA approved recall letter was distributed to all distribution points, and the recall process was initiated.

 

Reporting side effects

Public and healthcare professionals are encouraged to report any side effects after using a health product or after immunisation by using the Med Safety App. Your report will contribute to our monitoring of these health products.

Download latest version
Version: 1
Date Updated: 29/07/2026
File Type: www
Category: Product Recall
Unit: General ECTD & human medicines, Regulatory Compliance