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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
Related Medical Device Recalls
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Product Description
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Z-1677-2023 - DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212724 2 06/02/2023 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-1678-2023 - DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212725 2 06/02/2023 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-1681-2023 - DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212723 2 06/02/2023 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-1680-2023 - DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212722 2 06/02/2023 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-1679-2023 - DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212726 2 06/02/2023 DePuy Mitek, Inc., a Johnson & Johnson Co.
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