DePuy Mitek, Inc., a Johnson & Johnson Co.: Medical Device Recalls in 2023

Updated on March 25, 2026.

According to to data from the FDA, there were 5 medical device recalls made by DePuy Mitek, Inc., a Johnson & Johnson Co. in 2023. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212722
DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212725
DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212723
DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212726
DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212724