Every recall we track for Wright Medical Technology, Inc. — 29 in all — plus the complaints and injury reports the public filed about them.
Stryker recalls specific lots of Infinity Resection Adjustment Blocks for ankle surgery due to missing internal screw that could affect joint alignment during procedures.
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.
Wright Medical recalls Ortholoc 3Di Fusion plates with incorrect dorsiflexion laser markings. This could lead to improper bone alignment during surgery. Affected units have specific lot numbers.
Wright Medical recalls specific OrthoLoc 3Di Fusion plates with incorrect dorsiflexion laser markings. Affected units may have improper alignment risks during bone surgery.
Wright Medical recalls ORTHOLOC 3DSi CLAW II 4-hole plates (Size 25mm, REF 402S0425) sold with incorrect model numbers. Affected units may have wrong product in packaging, but no safety risk exists.
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.
Stryker recalls left plasma spray tibial trays with oversized lock detail. This may cause improper fit during surgery. Affected models include REF 200252904, Size 4.
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.
Wright Medical recalls EVOLVE Proline Stem implants with incorrect sizes in packaging. Affected lots contain mismatched stems that could lead to improper fitting during surgery.
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.
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.
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.
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.
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 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 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 Medical recalls Stryker CLAW II ORTHOLOC 3DSi plates with incorrect product in packaging. Affected units have specific model and lot numbers. No action needed as the hazard is packaging error, not a product defect.
Wright Medical recalls Charlotte MTP Hex Screw Model 411: Incorrect product in packaging. Affected units sold with specific lot numbers. Contact for replacement.
Wright Medical recalls Stryker DARCO Screw (REF DC2825016) due to incorrect product in packaging. Affected units may contain wrong item; contact for details.
Wright Medical recalls INBONE Total Ankle System (Model 220222210E) due to mismatched package contents and labeling. Affected units sold with specific lot codes.
Wright Medical recalls INBONE Total Ankle System (Model 220223214E) due to mismatched package contents and labeling. Affected units sold with specific lot codes.
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 Medical recalls hardware removal kit (Part 1985KIT1) with lot codes 01-64, 66-67 due to missing drivers for Dart-Fire screws. This may cause incomplete screw removal during foot and ankle procedures.
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 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 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 Medical Technology recalls VALOR Nail (Right, Small) with possible missing compression screw. Affected units may require replacement to prevent injury.
Wright Medical recalls VALOR Nail (Right, Medium) with potential missing compression screw. Affected units may need repair or replacement to prevent injury.
