Recall No : | PR090024 |
Date : | 21 August 2009 |
Name of Product : | M-Action |
Batch No : | CA009A08F |
Expiry Date : | 15/01/2011 |
Pack Size : | 10 capsules/box and 2 capsules/box |
Class of Recall : | 2 |
Level of Recall : | Retail |
Local Company : | Neucor Holdings Pte Ltd |
Manufacturer : | Hua Sun Medical Manufacturing Sdn Bhd |
Country of Manufacture : | Malaysia |
Reason for Recall : | Contained Desmethylacetildenafil and Acetilacid |
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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. |
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