Wright Medical Technology recalls
16 official recalls and safety alerts involving Wright Medical Technology since 2021-12, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Wright Medical Technology or the relevant agency.
- 2026-10-07
USWright Medical Technology, Inc. recalls CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating System
Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads, which if used would prevent a secure rigid engagement with the…
FDA · DeviceWright Medical Technology, Inc.US Nationwide distribution in the states of FL, TX, PA, CA, ID, MI, OK, TN,…Official notice →- 2024-04-10
- US
Wright Medical Technology, Inc. recalls stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument…
FDA · DeviceWright Medical Technology, Inc.US: TX, NE, and AUSTRALIA, BELGIUM, BRAZIL, CANADA, CHINA, COLOMBIA, FRANCE,…Official notice → - 2023-07-12
- US
Wright Medical Technology, Inc. recalls Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.
The devices were manufactured with the pin sleeve holes too narrow, which does not allow the pin sleeves to pass through the pin sleeve holes, thereby preventing pin placement through the pin holes.
FDA · DeviceWright Medical Technology, Inc.There was no U.S. distribution, including government and military. Foreign…Official notice → - 2023-05-03
- US
Wright Medical Technology, Inc. recalls stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
- 2023-03-08
- US
Wright Medical Technology, Inc. recalls ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device
Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for…
FDA · DeviceWright Medical Technology, Inc.US Nationwide distribution in the state of NY.Official notice → - 2022-11-02
- US
Wright Medical Technology, Inc. recalls Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3
The tibial tray lock detail is oversized (larger than specification).
FDA · DeviceWright Medical Technology, Inc.US Nationwide distribution in the state of New York.Official notice → - 2022-10-12
- US
Wright Medical Technology, Inc. recalls stryker EVOLVE, Proline Stem, CoCr, Size: +4, OD: 9.5mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System…
The outer label does not match the device inside the package. The affected lot of EVOLVE Proline Stem 7.5mm +2 contains a size 9.5mm +4 stem, while the affected lot of EVOLVE Proline Stem 9.5mm +4 contains a size 7.5mm…
- 2022-08-31
- US
Wright Medical Technology, Inc. recalls Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.
An incorrect sizing label was applied to the carton packaging.
FDA · DeviceWright Medical Technology, Inc.Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice → - 2022-07-20
- US
Wright Medical Technology, Inc. recalls Wright EVOLVE TRIAD Plate Cutter, REF 49510120
The plate cutter is unable to meet sterilization requirements when it is sterilized in a double-wrapped configuration according to the Option 1 Steam Sterilization parameters detailed in instructions for use
FDA · DeviceWright Medical Technology, Inc.Nationwide and PR, and Australia, Canada, Chile, Colombia, Hong Kong, Puerto…Official notice → - 2022-07-06
- US
Wright Medical Technology, Inc. recalls Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the INFINITY Total…
The instrument is incorrectly color coded.
FDA · DeviceWright Medical Technology, Inc.Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice → - 2022-04-06
- US
Wright Medical Technology, Inc. recalls EasyFuse Dynamic Compression System Instrument Pack
The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
FDA · DeviceWright Medical Technology, Inc.US distribution to Florida, North Carolina, Ohio, and TexasOfficial notice → - 2022-03-23
- US
Wright Medical Technology, Inc. recalls Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC…
An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.
FDA · DeviceWright Medical Technology, Inc.International distribution to the country of France.Official notice → - 2022-03-09
- US
Wright Medical Technology, Inc. recalls The DARCO¿ Locking Bone Plate System is designed with rhombus (parallelogram) plates of biocompatible titanium. The plates use…
Product was labelled with the incorrect manufacturing and distribution dates.
FDA · DeviceWright Medical Technology, Inc.International distribution in the countries of Japan and the United Kingdom.Official notice → - 2021-12-29
- US
Wright Medical Technology, Inc. recalls Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE Lisfranc…
Incorrect product is contained in the packaging.
FDA · DeviceWright Medical Technology, Inc.Worldwide distribution - US Nationwide distribution in the states of AZ, IA,…Official notice → - US
Wright Medical Technology Inc recalls Stryker DARCO Screw, Locking, Ti6A14V, REF DC2825016, 2.7mm x 16mm.
The incorrect product is contained in the packaging.
FDA · DeviceWright Medical Technology IncWorldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The…Official notice → - 2021-12-08
- US
Wright Medical Technology Inc recalls INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS
The package contents and package labeling do not match.
FDA · DeviceWright Medical Technology IncUS Nationwide distribution in the states of MI and PA.Official notice →