Wright Medical Technology, Inc. recalls
Every recall we track for Wright Medical Technology, Inc. — 30 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Wright Medical Technology, Inc. peaked in 2022 (10); 30 since 2017.
All FDA recall records for Wright Medical Technology, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 2 | 0 | 2 |
| 2019 | 0 | 0 | 2 | 0 | 2 |
| 2020 | 0 | 0 | 4 | 0 | 4 |
| 2021 | 0 | 0 | 4 | 1 | 5 |
| 2022 | 0 | 1 | 9 | 0 | 10 |
| 2023 | 0 | 0 | 5 | 0 | 5 |
| 2024 | 0 | 1 | 0 | 0 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
Most common reasons for Wright Medical Technology, Inc. recalls
What to do if you have a recalled Wright Medical Technology, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Wright Medical Technology, Inc. recalls
21 shown- Use cautionMedical device
Wright Medical Technology, Inc. recalls CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating System
Wright Medical Technology recalls 34 Charlotte Claw Screws (Lot 1826666) distributed August 2025-April 2026. Missing threads may cause surgery delays or alternative procedures.
Wright Medical TechnologyAug 18, 2026 - Use cautionMedical device
Wright Medical Technology, Inc. recalls stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
Stryker recalls specific lots of Infinity Resection Adjustment Blocks for ankle surgery due to missing internal screw that could affect joint alignment during procedures.
StrykerMar 6, 2024 - Lower riskMedical device
Wright Medical Technology, Inc. recalls Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.
Stryker recalls Infinity Alignment Frame Distal Sub-Assembly (Catalog #33600020) due to pin sleeve holes being too narrow, preventing proper pin placement. Affected units include specific lot numbers.
StrykerJun 13, 2023 - Lower riskMedical device
Wright Medical Technology, Inc. recalls stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
Wright Medical recalls specific OrthoLoc 3Di Fusion plates with incorrect dorsiflexion laser markings. Affected units may have improper alignment risks during bone surgery.
Wright MedicalApr 10, 2023 - Lower riskMedical device
Wright Medical Technology, Inc. recalls ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device
Wright Medical recalls ORTHOLOC 3DSi CLAW II 4-hole plates (Size 25mm, REF 40241425) sold with incorrect lot numbers. This mix-up means some packages contain the wrong product model.
Wright MedicalFeb 2, 2023 - Lower riskMedical device
Wright Medical Technology, Inc. recalls Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3
Stryker recalls left plasma spray tibial trays with oversized lock detail that may cause improper fit during surgery. Affected units include specific model and lot codes.
StrykerSep 30, 2022 - Lower riskMedical device
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
Wright Medical recalls EVOLVE Proline Stem implants with incorrect sizes in packaging. Affected lots contain mismatched stem sizes that could lead to improper fitting during surgery.
Wright MedicalAug 3, 2022 - Lower riskMedical device
Wright Medical Technology, Inc. recalls Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.
Stryker recalls finger joint implants with incorrect sizing labels on packaging. Affected units may be mislabeled, but no immediate safety risk exists. Contact Stryker for details.
StrykerJul 27, 2022 - Lower riskMedical device
Wright Medical Technology, Inc. recalls Wright EVOLVE TRIAD Plate Cutter, REF 49510120
Wright Medical recalls specific models of EVOLVE TRIAD Plate Cutters that may not meet sterilization standards when double-wrapped for steam sterilization, posing infection risks during medical procedures.
Wright MedicalJun 14, 2022 - Lower riskMedical device
Wright Medical Technology, Inc. recalls Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the
Stryker recalls INFINITY Resect Guide for INBONE Talus, Size 4 (Model #33620254) due to incorrect color coding. This may cause confusion during surgical procedures. Affected units were sold with Lot #2039558 and GTIN 00889797006552.
StrykerJun 2, 2022 - Use cautionMedical device
Wright Medical Technology, Inc. recalls EasyFuse Dynamic Compression System Instrument Pack
Wright Medical recalls EasyFuse Dynamic Compression System Instrument Packs with model FFSP1530 that may jam during surgery, causing drill guide breakage. Affected units have specific lot codes and expiration dates.
Wright MedicalMar 10, 2022 - Lower riskMedical device
Wright Medical Technology, Inc. recalls Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the
Wright Medical recalls ORTHOLOC Non-Locking Screws (2mm x 8mm) due to incorrect screw packaging. This component is part of the ORTHOLOC 2.0/2.4 Plate System and may contain a locking screw instead of non-locking.
Wright Medical TechnologyFeb 15, 2022 - Lower riskMedical device
Wright Medical Technology, Inc. recalls The DARCO¿ Locking Bone Plate System is designed with rhombus (parallelogram) plates of biocompatible titanium. The
Wright Medical recalls DARCO Locking Bone Plate System due to incorrect manufacturing and distribution dates on labels. Affected units may have safety risks if used without proper date verification.
Wright MedicalFeb 9, 2022 - Lower riskMedical device
Wright Medical Technology, Inc. recalls Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE
Wright Medical recalls Charlotte MTP Hex Screw Model 411: Incorrect product in packaging. Affected units sold with specific lot numbers. Contact for replacement.
Wright MedicalDec 3, 2021 - Lower riskMedical device
Wright Medical Technology Inc recalls Stryker DARCO Screw, Locking, Ti6A14V, REF DC2825016, 2.7mm x 16mm.
Wright Medical recalls Stryker DARCO Screw (REF DC2825016) due to incorrect product in packaging. Affected units may contain wrong item; contact for details.
Wright MedicalDec 3, 2021 - UnratedMedical device
Wright Medical Technology Inc recalls INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS
Wright Medical recalls INBONE Total Ankle System (Model 220223214E) due to mismatched package contents and labeling. Affected units sold with specific lot codes.
Wright MedicalNov 4, 2021 - Lower riskMedical device
Wright Medical Technology Inc recalls EVOLVE STEM 8.5MM Model # 496S085
Wright Medical recalls EVOLVE STEM 8.5MM Model 49:496S085 due to lack of sterility assurance. Affected units may pose infection risks during medical procedures.
Wright MedicalAug 26, 2020 - Lower riskMedical device
Wright Medical Technology, Inc. recalls Screw Removal Case Assembly, Part Number 1985BASE - Product Usage: The Wright Medical hardware removal kit is designed
Wright Medical recalls a hardware removal kit for foot and ankle procedures that lacks drivers for Dart-Fire screws. This could lead to incomplete hardware removal during surgery. Affected kits have part number 1985BASE and were sold for medical use.
Wright MedicalJul 28, 2020 - Lower riskMedical device
Wright Medical Technology Inc recalls WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left, REF 2000252902 - Product Usage: is intended to give a patient
Wright Medical recalls a specific lot of INBONE Tibial Trays due to missing plasma coating. This may affect patient mobility and joint function. Contact for details.
Wright MedicalApr 9, 2020 - Lower riskMedical device
Wright Medical Technology, Inc. recalls WRIGHT EVOLVE Proline Head, Size: +2, OD: 20mm, REF 496H220
Wright Medical recalls EVOLVE Proline Head Size +2, OD 20mm (REF 496H220) due to incorrect labeling and laser marking. Affected units may have wrong size product.
Wright MedicalDec 27, 2019 - Lower riskMedical device
Wright Medical Technology, Inc. recalls WRIGHT, Wright Medical Technology, VALOR(R) Nail, Right, Medium, OD: 10mm, L: 200mm, REF415101020
Wright Medical recalls VALOR Nail (Right, Medium) with potential missing compression screw. Affected units may need repair or replacement to prevent injury.
Wright MedicalMar 14, 2018
Wright Medical Technology, Inc. recall questions
How many recalls has Wright Medical Technology, Inc. had?
30 recalls from Wright Medical Technology, Inc. are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Wright Medical Technology, Inc. recall?
Wright Medical Technology, Inc. recalls CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating System, dated Aug 18, 2026. Every Wright Medical Technology, Inc. recall is listed on this page, newest first.
Why are Wright Medical Technology, Inc. products recalled?
The most common reasons on record: The incorrect product is contained in the packaging. (2); The package contents and package labeling do not match. (2); The tibial tray lock detail is oversized (larger than specification). (2).
What should I do if I have a recalled Wright Medical Technology, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Wright Medical Technology, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.