Class I - Dangerous
The sterilization process used was unqualified.
The sterilization process used was unqualified.
The sterilization process used was unqualified.
The firm received a customer complaint of observed spots on the wipes. The manufacturer confirmed that the product had bacterial contamination. This leads to a potential risk of infection.
The recalling firm received a customer complaint stating the tape was difficult to peel off the roll and had poor adhesion.