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Soothe 800 Capsule

Recall No :
PR100017
Date : 
24 November 2010
Name of Product : 
Soothe 800 capsule
Batch No :
37828
Expiry Date :
08/2012
Pack Size : 
120 capsules
Class of Recall :  
2
Level of Recall :  
Retail
Product Licence No : SIN07514P
Local Company : 
Chong Park Medical Hall (Singapore) Pte Ltd
Manufacturer : 
Beacons Pharmaceuticals Pte Ltd
Country of Manufacture :
Singapore
Reason for Recall : 
The contents of Caffeine and Salicylamide were found to be understrength.


Class of Recall
 
Class 1 recall is initiated when the product defect poses a life-threatening situation to users. Some examples of defects that will result in a Class 1 recall are non-sterile injections, contamination with toxic substances and products with major labelling errors.
 
Class 2 recall is initiated when the problem or defect is unlikely to cause serious harm to users. Some examples of defects that will result in a Class 2 recall include products with minor labelling errors or products which fail to meet product specification or pharmacopoeia standards but are likely to cause minimal hazard to users.
 


Last updated on 26 Nov 2010 11:39:48
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