Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K150209 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft tissue to bone fixation in assoc... | 2 | 06/02/2023 | DePuy Mitek, Inc., a Johnson & Johnson Co. |
DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft tissue to bone fixation in associ... | 2 | 06/02/2023 | DePuy Mitek, Inc., a Johnson & Johnson Co. |
DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft tissue to bone fixation in associatio... | 2 | 06/02/2023 | DePuy Mitek, Inc., a Johnson & Johnson Co. |
DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft tissue to bone fixation in association... | 2 | 06/02/2023 | DePuy Mitek, Inc., a Johnson & Johnson Co. |
DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft tissue to bone fixation in association ... | 2 | 06/02/2023 | DePuy Mitek, Inc., a Johnson & Johnson Co. |
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