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Wright Medical Technology Recalls
78 recalls on record · November 7, 2012 to April 10, 2024 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 10, 2024Medical DevicesFDA
Wright Medical Technology, Inc. recalls stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
Hazard: 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 assembly. The missing screw is used to lockout the Medial/Lateral adjustment on the INFINITY Resection Adjustment Guide.
July 12, 2023Medical DevicesFDA
Wright Medical Technology, Inc. recalls Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.
Hazard: 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.
May 3, 2023Medical DevicesFDA
Wright Medical Technology, Inc. recalls stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
Hazard: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
May 3, 2023Medical DevicesFDA
Wright Medical Technology, Inc. recalls stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation
Hazard: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
March 8, 2023Medical DevicesFDA
Wright Medical Technology, Inc. recalls ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device
Hazard: 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 402S0425 incorrectly contained 40241425, and vice versa.
March 8, 2023Medical DevicesFDA
Wright Medical Technology, Inc. recalls ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone fixation device
Hazard: 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 402S0425 incorrectly contained 40241425, and vice versa.
November 2, 2022Medical DevicesFDA
Wright Medical Technology, Inc. recalls Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 18mm Stem Base, REF 200252904, Size 4
Hazard: The tibial tray lock detail is oversized (larger than specification).
November 2, 2022Medical DevicesFDA
Wright Medical Technology, Inc. recalls Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3
Hazard: The tibial tray lock detail is oversized (larger than specification).
October 12, 2022Medical DevicesFDA
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 Rep
Hazard: 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 +2 stem.
October 12, 2022Medical DevicesFDA
Wright Medical Technology, Inc. recalls stryker EVOLVE, Proline Stem, CoCr, Size: +2, O: 705mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repai
Hazard: 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 +2 stem.
August 31, 2022Medical DevicesFDA
Wright Medical Technology, Inc. recalls Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.
Hazard: An incorrect sizing label was applied to the carton packaging.
July 20, 2022Medical DevicesFDA
Wright Medical Technology, Inc. recalls Wright EVOLVE TRIAD Plate Cutter, REF 49510120
Hazard: 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
July 6, 2022Medical DevicesFDA
Wright Medical Technology, Inc. recalls Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the INFINI
Hazard: The instrument is incorrectly color coded.
April 6, 2022Medical DevicesFDA
Wright Medical Technology, Inc. recalls EasyFuse Dynamic Compression System Instrument Pack
Hazard: The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
March 23, 2022Medical DevicesFDA
Wright Medical Technology, Inc. recalls Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the OR
Hazard: An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.
March 9, 2022Medical DevicesFDA
Wright Medical Technology, Inc. recalls The DARCO¿ Locking Bone Plate System is designed with rhombus (parallelogram) plates of biocompatible titanium. The pla
Hazard: Product was labelled with the incorrect manufacturing and distribution dates.
December 29, 2021Medical DevicesFDA
Wright Medical Technology, Inc. recalls Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE Lisf
Hazard: Incorrect product is contained in the packaging.
December 29, 2021Medical DevicesFDA
Wright Medical Technology Inc recalls Stryker DARCO Screw, Locking, Ti6A14V, REF DC2825016, 2.7mm x 16mm.
Hazard: The incorrect product is contained in the packaging.
December 29, 2021Medical DevicesFDA
Wright Medical Technology Inc recalls Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
Hazard: The incorrect product is contained in the packaging.
December 8, 2021Medical DevicesFDA
Wright Medical Technology Inc recalls INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS
Hazard: The package contents and package labeling do not match.
December 8, 2021Medical DevicesFDA
Wright Medical Technology Inc recalls INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUS
Hazard: The package contents and package labeling do not match.
September 30, 2020Medical DevicesFDA
Wright Medical Technology Inc recalls EVOLVE STEM 8.5MM Model # 496S085
Hazard: Lack of sterility assurance
August 19, 2020Medical DevicesFDA
Wright Medical Technology, Inc. recalls Screw Removal Case Assembly, Part Number 1985BASE - Product Usage: The Wright Medical hardware removal kit is designed t
Hazard: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws.
August 19, 2020Medical DevicesFDA
Wright Medical Technology, Inc. recalls Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to facil
Hazard: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws.
May 13, 2020Medical DevicesFDA
Wright Medical Technology Inc recalls WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left, REF 2000252902 - Product Usage: is intended to give a patient li
Hazard: One lot of INBONE Tibial Trays is missing the plasma coating.
February 12, 2020Medical DevicesFDA
Wright Medical Technology, Inc. recalls WRIGHT EVOLVE Proline Head, Size: +2, OD: 22mm, REF 496H222
Hazard: Two lots of EVOLVE Modular Radial Head could have the wrong size product in the package. Both the label and laser marking are incorrect on the affected product.
February 12, 2020Medical DevicesFDA
Wright Medical Technology, Inc. recalls WRIGHT EVOLVE Proline Head, Size: +2, OD: 20mm, REF 496H220
Hazard: Two lots of EVOLVE Modular Radial Head could have the wrong size product in the package. Both the label and laser marking are incorrect on the affected product.
December 4, 2019Medical DevicesFDA
Wright Medical Technology, Inc. recalls CPS CALCANEAL PLATE SML 54MM, Part Number DCS2805001
Hazard: The firm discovered a lack of adequate documentation confirming sterility on certain products.
December 4, 2019Medical DevicesFDA
Wright Medical Technology, Inc. recalls SWANSON TRAPEZIUM IMPLANT, Part Number 4520002
Hazard: The firm discovered a lack of adequate documentation confirming sterility on certain products.
December 4, 2019Medical DevicesFDA
Wright Medical Technology, Inc. recalls SWANSON FINGER JOINT #2, Part Number 4700002
Hazard: The firm discovered a lack of adequate documentation confirming sterility on certain products.