Artibase Suspension (Artemether and Lumefantrine for oral Suspension
Summary
Date Recall was issued:
Product Name:
Manufacturer:
Recalling Firm:
Batch(es):
Manufacturing Date:
Expiry Date:
Reason for Recall:
9th January 2025Â
Artibase Suspension (Artemether and Lumefantrine for oral SuspensionÂ
Base Pharmacy Co. Limited, IndiaÂ
Base Pharmacy Co. LtdÂ
A-147013Â
06/2023 Â
05/ 2025 Â
Substandard product, failed Assay for Artemether and Lumefantrine as per the acceptance criteria in the International PharmacopoeiaÂ
Announcement
This recall is necessitated as a result of warehouse market surveillance conducted at the warehouse. Actual product specification is a powder for oral suspension. The affected batches were caked and not free flowing. This makes the product substandard and therefore not recommended for its intended use.
