Product Recalls
Recall of Bepraz Gastro Resistant Tablets 20mg (Rabeprazole)
Audiences
Healthcare professional
Product type
Therapeutic Products
25 August 2025
Consumer level recall of five batches of Bepraz Gastro Resistant Tablet 20mg due to detection of low levels of an impurity
This article has been migrated from an earlier version of the site and may display formatting inconsistencies.
Recall details
Date of Recall: | 13 Aug 2025 |
|---|---|
Product: | Bepraz Gastro Resistant Tablets 20mg |
Active Ingredients: | Rabeprazole Sodium 20mg |
Product Category: | Therapeutic product |
Registration Number: | SIN15259P |
Batch No.: | PTE5026A |
Class of Recall: | 2 |
Level of Recall: | Consumer |
Local Company: | Ranbaxy (Malaysia) Sdn. Bhd |
Description of Issue: | Detection of low levels of an impurity, a degradation by-product of the active ingredient, in one batch. As a precautionary measure, the manufacturer, Sun Pharmaceutical, is recalling all five batches of Bepraz currently available in the market. There is no immediate cause for concern given the low levels of impurity, which has no evidence of harm. |
Recall Instructions: | Patients: |
Note:
The Health Sciences Authority (HSA) publishes information regarding recalls of health products supplied in Singapore. These product recalls may be conducted on a company’s own initiative or upon HSA’s request to remove products where there are issues with quality, safety or efficacy.
When a recall is initiated, it does not necessarily imply that a product is considered unsafe or is inefficacious. A recall can also be initiated to remove products with quality defects that does not impact safety or efficacy from the market so as to ensure that products registered in Singapore continue to meet the stringent regulatory standards stipulated by HSA.
Not all recalls will lead to press releases. However, when a recall involves a product that has been widely distributed or a product that poses a serious health risk, HSA will issue a press release to inform members of public.
Class of recall
A recall is classified as Class 1 or Class 2 depending on the potential hazard of the issue.
Class 1: For recalls of products with issues that can potentially cause serious adverse health outcomes or death.
Class 2: For recalls of products with issues that would not likely cause serious adverse health outcomes.
Level of recall
The level of product recall will depend on the potential hazard of the affected product, extent of distribution and whether other mitigating measures can be taken to address the issue.
Consumer level: Affected product or batch(es) recalled from patients and consumers as well as wholesale suppliers, retail suppliers, hospitals, clinics and pharmacies.
Retail level: Affected product or batch(es) recalled from retail suppliers, hospitals, clinics and pharmacies as well as wholesale suppliers.
Wholesale level: Affected product or batch(es) recalled from wholesale suppliers.