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All product recalls associated with Steris Corporation Hopkins Facility.
Total Recalls
2
Past Year
0
Class I (Serious)
0
Most Recent
Aug 2022
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Product contains incorrect chemical indicators in packaging.
Loose or missing adaptor: The center insert of the adaptor #6 restrictor could become loose and/or come out of the adaptor's housing. The absence of adaptor #6's center insert may affect the sterilization process of the attached endoscope.