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All product recalls associated with DePuy Mitek, Inc., a Johnson & Johnson Co..
Total Recalls
4
Past Year
2
Class I (Serious)
0
Most Recent
Feb 2025
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.
Device is missing the pin in the graft loader component.
Device is missing the pin in the graft loader component.
IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS Anchor inserter tip detected during surgery may require removal, potentially causing bone damage and longer surgery time