--- title: "Wright Medical Technology Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Wright Medical Technology Inc recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/wright-medical-technology-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Wright Medical Technology Inc recall records **14** reported ongoing 21 records in this archive. Latest source date Mar 6, 2024. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Mar 6, 2024 FDA device enforcement ### [stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty](https://isitonrecall.com/recall/fda-device-z-1477-2024-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 assembly. The missing screw is used to ... Class II Reported ongoing Distribution: US: TX, NE, and AUSTRALIA, BELGIUM, BRAZIL, CANADA, CHINA, COLOMBIA, FRANCE, GERMANY, ITALY, SPAIN, SWEDEN, SWITZERLAND, UK [Official source for stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1477-2024%22) Jun 13, 2023 FDA device enforcement ### [Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.](https://isitonrecall.com/recall/fda-device-z-2105-2023-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. Class II Reported ongoing Distribution: There was no U.S. distribution, including government and military. Foreign distribution was made to Australia, Belgium, Canada, Chile, China, Colombia, France, Germany, Italy, M... [Official source for Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2105-2023%22) Apr 10, 2023 FDA device enforcement ### [stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation](https://isitonrecall.com/recall/fda-device-z-1466-2023-stryker-ortholoc-3di-fusion-plate-mtp-right-ref-58a220rt-bone-stabilization-and-fixation/) Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1466-2023%22) Apr 10, 2023 FDA device enforcement ### [stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation](https://isitonrecall.com/recall/fda-device-z-1467-2023-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. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1467-2023%22) Feb 2, 2023 FDA device enforcement ### [ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone fixation device](https://isitonrecall.com/recall/fda-device-z-1169-2023-ortholoc-3dsi-claw-ii-4-hole-plate-size-25mm-ref-402s0425-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 402S0425 incorrectly contained 40241425, and... Class II Reported ongoing Distribution: US Nationwide distribution in the state of NY. [Official source for ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone fixation device](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1169-2023%22) Feb 2, 2023 FDA device enforcement ### [ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device](https://isitonrecall.com/recall/fda-device-z-1170-2023-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 402S0425 incorrectly contained 40241425, and... Class II Reported ongoing Distribution: US Nationwide distribution in the state of NY. [Official source for ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1170-2023%22) Sep 30, 2022 FDA device enforcement ### [Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3](https://isitonrecall.com/recall/fda-device-z-0139-2023-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). Class II Reported terminated Distribution: US Nationwide distribution in the state of New York. [Official source for Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0139-2023%22) Sep 30, 2022 FDA device enforcement ### [Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 18mm Stem Base, REF 200252904, Size 4](https://isitonrecall.com/recall/fda-device-z-0140-2023-stryker-inbone-tibial-tray-left-plasma-spray-ti6al4v-cpti-use-w-18mm-stem-base-ref-200252904-size-4/) The tibial tray lock detail is oversized (larger than specification). Class II Reported terminated Distribution: US Nationwide distribution in the state of New York. [Official source for Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 18mm Stem Base, REF 200252904...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0140-2023%22) Aug 3, 2022 FDA device enforcement ### [stryker EVOLVE, Proline Stem, CoCr, Size: +2, O: 705mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System is a set configuration designed to address radial...](https://isitonrecall.com/recall/fda-device-z-0005-2023-stryker-evolve-proline-stem-cocr-size-2-o-705mm-ref-496s275-wright-s-evolve-proline-plus-radial-head/) 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. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for stryker EVOLVE, Proline Stem, CoCr, Size: +2, O: 705mm, REF 496S275, Wright s EVOLVE Proline Plus...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0005-2023%22) Aug 3, 2022 FDA device enforcement ### [stryker EVOLVE, Proline Stem, CoCr, Size: +4, OD: 9.5mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System is a set configuration designed to address radia...](https://isitonrecall.com/recall/fda-device-z-0006-2023-stryker-evolve-proline-stem-cocr-size-4-od-9-5mm-ref-496s275-wright-s-evolve-proline-plus-radial-hea/) 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. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for stryker EVOLVE, Proline Stem, CoCr, Size: +4, OD: 9.5mm, REF 496S275, Wright s EVOLVE Proline Plu...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0006-2023%22) Jul 27, 2022 FDA device enforcement ### [Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.](https://isitonrecall.com/recall/fda-device-z-1567-2022-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. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of AZ, CA, FL, GA, NY, PA, and TN. The countries of the Australia, France, the Netherlands, Sweden, and the Uni... [Official source for Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1567-2022%22) Jun 14, 2022 FDA device enforcement ### [Wright EVOLVE TRIAD Plate Cutter, REF 49510120](https://isitonrecall.com/recall/fda-device-z-1366-2022-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 Class II Reported ongoing Distribution: Nationwide and PR, and Australia, Canada, Chile, Colombia, Hong Kong, Puerto Rico [Official source for Wright EVOLVE TRIAD Plate Cutter, REF 49510120](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1366-2022%22) Jun 2, 2022 FDA device enforcement ### [Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the INFINITY Total Ankle System.](https://isitonrecall.com/recall/fda-device-z-1291-2022-stryker-infinity-resect-guide-for-inbone-talus-size-4-model-33620254-non-sterile-an-instrument-used/) The instrument is incorrectly color coded. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, CT, FL, GA, IA, IL, MA, MI, MN, MO, NC, NY, OH, PA, TX, and WA. The countries of Australia, Belg... [Official source for Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrume...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1291-2022%22) Mar 10, 2022 FDA device enforcement ### [EasyFuse Dynamic Compression System Instrument Pack](https://isitonrecall.com/recall/fda-device-z-0853-2022-easyfuse-dynamic-compression-system-instrument-pack/) The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking. Class II Reported terminated Distribution: US distribution to Florida, North Carolina, Ohio, and Texas [Official source for EasyFuse Dynamic Compression System Instrument Pack](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0853-2022%22) Feb 15, 2022 FDA device enforcement ### [Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC 2.0/2.4 Plate System.](https://isitonrecall.com/recall/fda-device-z-0786-2022-wright-medical-technology-inc-ortholoc-non-locking-screw-2mm-x-8mm-ref-5201120008-non-sterile-a-comp/) An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw. Class II Reported terminated Distribution: International distribution to the country of France. [Official source for Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0786-2022%22) Feb 9, 2022 FDA device enforcement ### [The DARCO¿ Locking Bone Plate System is designed with rhombus (parallelogram) plates of biocompatible titanium. The plates use either 2.7mm or 3.5mm screws which intersect each ...](https://isitonrecall.com/recall/fda-device-z-0679-2022-the-darco-locking-bone-plate-system-is-designed-with-rhombus-parallelogram-plates-of-biocompatible-t/) Product was labelled with the incorrect manufacturing and distribution dates. Class II Reported terminated Distribution: International distribution in the countries of Japan and the United Kingdom. [Official source for The DARCO¿ Locking Bone Plate System is designed with rhombus (parallelogram) plates of biocompat...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0679-2022%22) Dec 3, 2021 FDA device enforcement ### [Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.](https://isitonrecall.com/recall/fda-device-z-0392-2022-stryker-claw-ii-ortholoc-3dsi-plate-hole-qty-4-30mm-ref-40240430/) The incorrect product is contained in the packaging. Class II Reported ongoing Distribution: Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom. [Official source for Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0392-2022%22) Dec 3, 2021 FDA device enforcement ### [Stryker DARCO Screw, Locking, Ti6A14V, REF DC2825016, 2.7mm x 16mm.](https://isitonrecall.com/recall/fda-device-z-0393-2022-stryker-darco-screw-locking-ti6a14v-ref-dc2825016-2-7mm-x-16mm/) The incorrect product is contained in the packaging. Class II Reported ongoing Distribution: Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom. [Official source for Stryker DARCO Screw, Locking, Ti6A14V, REF DC2825016, 2.7mm x 16mm.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0393-2022%22) Dec 3, 2021 FDA device enforcement ### [Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE Lisfranc Reconstruction System.](https://isitonrecall.com/recall/fda-device-z-0401-2022-wright-medical-technology-inc-charlotte-mtp-hex-screw-model-41122718-2-7mm-x-18mm-a-component-of-the/) Incorrect product is contained in the packaging. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of AZ, IA, and SC. The countries of Australia, Canada, Chile, Spain, and United Kingdom. [Official source for Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a componen...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0401-2022%22) Nov 4, 2021 FDA device enforcement ### [INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUS](https://isitonrecall.com/recall/fda-device-z-0315-2022-inbone-total-ankle-system-inbone-poly-insert-sz-2-10mm-sulcus/) The package contents and package labeling do not match. Class II Reported terminated Distribution: US Nationwide distribution in the states of MI and PA. [Official source for INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUS](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0315-2022%22) ## Reasons in these listed records - 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/L... - 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. - Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts. - 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. These examples come from this result page and are not a ranking of every recall reason. ## Checking Wright Medical Technology Inc ### Is there a recall on wright medical technology inc right now? This archive contains 21 records, including 14 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Wright Medical Technology Inc](https://isitonrecall.com/check/?q=Wright%20Medical%20Technology%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)