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Health Sciences Authority
Product Recalls

QING RE HOU TONG CAPSULE

Audiences

Healthcare professional

Industry member

Product type

Chinese Proprietary Medicines

2 September 2025

Retail-level recall of QING RE HOU TONG CAPSULE (Batch no.: C2306B; Expiry: 05/2026) due to Total Yeast and Mould count detected to exceed legislative limit.

This article has been migrated from an earlier version of the site and may display formatting inconsistencies.

Recall details

Date of Recall:

2 Sep 2025

Product:

QING RE HOU TONG CAPSULE

Product Category:

Chinese Proprietary Medicine

Batch No.:

C2306B

Class of Recall:

2

Level of Recall:

Retail

Local Company:

Tai Chong Fatt Medical Hall

Description of Issue:

The product was tested under HSA’s product quality surveillance programme and detected to contain Total Yeast and Mould Count exceeding legislative limit

Recall Instructions:

Retail and wholesale suppliers:
Stop supplying the affected batch and return the remaining stocks to the company.

PlaQing Re Hou Tong Capsule box showing front label with Chinese and English textceholder
Qing Re Hou Tong Capsule box showing back label with dosage and ingredients

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.

  1. Consumer level: Affected product or batch(es) recalled from patients and consumers as well as wholesale suppliers, retail suppliers, hospitals, clinics and pharmacies.

  2. Retail level: Affected product or batch(es) recalled from retail suppliers, hospitals, clinics and pharmacies as well as wholesale suppliers.

  3. Wholesale level: Affected product or batch(es) recalled from wholesale suppliers.

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