Recall of Clonotril (Clonazepam) 0.5 Tablet 0.5 mg
12 October 2026
Audiences
Healthcare professional
Product-type
Therapeutic Products
Retail-level recall of several batches of Clonotril 0.5 Tablet 0.5 mg due to out-of-specification results in stability study
Recall details
Date of recall: | 12 October 2026 |
Product: | Clonotril 0.5 Tablet 0.5 mg |
Active Ingredient: | Clonazepam |
Product Category: | Therapeutic Product |
Registration Number: | SIN06410P |
Batch No.: | 99976 101777 101306 102820 103832 103833 104001 104377 106113 106114 106121 106539 107367 108506 108507 108508 109885 109886 110852 111227 112050 112287 114170 115066 115067 116357 118192 118294 118301 118747 118749 |
Class of Recall: | 2 |
Level of Recall: | Retail |
Local Company: | Goldplus Universal Pte Ltd |
Description of Issue: | Out-of-specification results in stability study |
Recall Instructions: | Hospitals, clinics, pharmacies: Stop supplying the affected batches and return the remaining stocks to the company. |
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 be publicly announced via press releases. When a recall involves a product that has been widely distributed or a product that poses a serious health risk, HSA will update the public through its channels, which may include its website, social media platforms or a press release.
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.
