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Medicine Quality Alert: Class II Recall of Cardoz 12.5 (Carvedilol 12.5 mg) Tablets, Batch no. GBC013001

Sai Pharmaceuticals Kenya Limited has initiated a voluntary recall of Cardoz 12.5 (Carvedilol 12.5 mg) Tablets, Batch no. GBC013001 Manufactured by Ipca Laboratories Limited, India.

From: Pharmacy and Poisons Board

Date of Recall Initiation: 14/11/2025

Recall Reference Number: REC/2025/035

Recall Classification: Class II

Recall Level: Retail/Facility level

Local Technical Representative: Sai Pharmaceuticals Kenya Limited

Manufacturer: Ipca Laboratories Limited

Product name: Cardoz 12.5

Active Pharmaceutical Ingredient: Carvedilol 12.5 mg

Affected counties: All

Affected Batch

Batch Number

Date of Manufacture

Date of expiry

Pack Size

   GBC013001

01/2023

12/2025

2 x 14 tablets

Brief description of the problem

The product is being recalled due to observed assay results of 94.7% against the specification limit of 95.0% to 105.0% at 24-month time point at storage condition 30°C/75%RH.

Action for healthcare professionals

Stop supplying the above batches immediately. Quarantine all remaining stock and await contact from Sai Pharmaceuticals Kenya Limited to arrange the return.

Action for patients and carers

No further action is required by patients as this is a Retail/hospital Pharmacy and Wholesaler/Distributor level recall. You are advised to talk to your healthcare professional if you have the above batch of Cardoz 12.5 (Carvedilol 12.5 mg) Tablets.

Further Information

For inquiries about consignments of the impacted batch, please contact Sai Pharmaceuticals Kenya Limite by email at: head-regulatory@saipharm.com Tel: 0721243322

You are advised to promptly report any case(s) of adverse events and suspected substandard and falsified products to the nearest healthcare facility or through the following channels:

For any further enquiries and feedback on the product recall, contact the post-marketing surveillance unit at the Pharmacy and Poisons Board via email at pms@ppb.go.ke

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