Manufacturer
78 recalls in our database name Wright Medical Technology, Inc. as the manufacturing or recalling firm.
Of the 78 recalls from Wright Medical Technology, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 4 (5%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Wright Medical Technology is recalling two lots of EVOLVE Modular Radial Heads because the product size in the package may be incorrect. Both labels and laser markings are wrong.
Wright Medical Technology is recalling 39 EVOLVE Modular Radial Heads because the product size inside the package does not match the label or laser marking.
Wright Medical Technology is recalling 65 units of INBONE STEM, TIBIAL, TOP components because adequate documentation confirming sterility was not found.
Wright Medical Technology is recalling 54 units of Valor Screws because adequate documentation confirming sterility was missing.
Wright Medical Technology is recalling 66 units of sterile headed drill bits because documentation confirming sterility was inadequate.
Wright Medical Technology is recalling 77 units of Dart Fire Headed Screws because the firm discovered a lack of adequate documentation confirming sterility.
Wright Medical Technology is recalling 18 units of Swanson Finger Joint #2 implants because documentation confirming sterility was inadequate.
Wright Medical Technology is recalling 30 Swanson Great Toe implants because the firm discovered a lack of adequate documentation confirming sterility.
Wright Medical Technology is recalling 42 units of CPS Calcaneal Plates because the firm discovered a lack of adequate documentation confirming sterility.
Wright Medical Technology is recalling 30 units of Evans Opening Wedge Plates because documentation confirming sterility was inadequate.
Wright Medical Technology is recalling 20 units of Swanson Finger Joint #1 implants because documentation confirming sterility was inadequate.
Wright Medical Technology is recalling 19 units of PRO-STIM 10cc Injectable because adequate documentation confirming sterility was missing.
Wright Medical Technology is recalling 40 units of Ortholoc 3DI locking screws because documentation confirming sterility was inadequate.
Wright Medical Technology is recalling 20 Swanson Trapezium Implants because the firm discovered a lack of adequate documentation confirming sterility.
Wright Medical Technology is recalling 47 units of VALOR Nails that may be missing an assembled compression screw.
Wright Medical Technology is recalling VALOR Nails that may be missing an assembled compression screw.
Wright Medical Technology is recalling 107 CrossCHECK Locking Screws because they may pass through the plate if excessive torque is applied, potentially causing intraoperative malfunction.
Wright Medical Technology is recalling 5,687 CrossCHECK Non-Locking Screws because they may pass through the plate if excessive torque is applied, potentially causing intraoperative malfunction.
Wright Medical Technology is recalling 126 units of PHALINX Hammertoe Handles because the term 'DORSAL' was laser etched on the incorrect side.
Wright Medical Technology is recalling 124 units of Phalinx Hammertoe Handles because the term DORSAL was laser etched on the incorrect side.
Wright Medical Technology is recalling 121 units of Phalinx Hammertoe Handles because the word 'DORSAL' was laser-etched on the incorrect side.
Wright Medical Technology is recalling 126 units of Phalinx Hammertoe Handles because the term DORSAL was laser etched on the incorrect side.
Wright Medical Technology is recalling 233 units of the Crosscheck Plating System because dimensional specifications are out of tolerance, posing a risk of intraoperative malfunction.
Wright Medical Technology is recalling 270 units of the Crosscheck Plating System because specific dimensions are out of specification, posing a risk of intraoperative malfunction.
Wright Medical Technology is recalling 100 units of Crosscheck Plating Systems because dimensional specifications are out of tolerance, posing a risk of intraoperative malfunction.
Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.
Wright Medical Technology (United States)
company in Memphis, United States
Source: Wikidata (Q30281365), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.