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Health Canada Medical devices

Five S 5.3

Issued August 16, 2023
Issue
Due to a failed revalidation of the sterilization process, there is no proof of the sterility of the products. The hazardous situation, that a contaminated product is used could lead to the consequence of patient infection. There is no subsequent risk to user or third parties. Recall start date: August 1, 2023
Hazard description
Sterility
Product
Product name
Five S 5.3
Reference
ID
RA-74136