Integra LifeSciences Recalls MicroMyst Applicators Over Sterility Risks Integra LifeSciences, a leading global medical technology company, has announced a voluntary recall of its MicroMyst Applicators due to potential concerns regarding sterility . The recall comes after an internal review revealed incomplete bioburden assessments (tests that check for microbes before sterilization) and missing documentation in the sterilization transfer process . These lapses could compromise sterility, creating risks of infection or inflammation for patients. About the Recall Product: MicroMyst® Applicator, packaged in boxes of 5. Catalog Number: 205000DS. Distribution: Worldwide – including the U.S., Canada, EU, Australia, Asia, and Latin America. Regulatory Action: FDA (U.S.): Class I recall (highest level). Health Canada: Type II recall. Why This Matters While no serious injuries have been reported so far, the potential for infection highlights the critical import...