PlainRecalls

Wright Medical Technology, Inc.

58 recalls on record · Latest: Apr 10, 2024

Wright Medical Technology, Inc. Recall Insight

Wright Medical Technology, Inc. appears on 58 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.069% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Apr 10, 2024, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Sep 17, 2014 to Apr 10, 2024.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Apr 10, 2024

stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty

FDA Devices Moderate Jul 12, 2023

Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.

FDA Devices Moderate May 3, 2023

stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation

FDA Devices Moderate May 3, 2023

stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation

FDA Devices Moderate Mar 8, 2023

ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device

FDA Devices Moderate Nov 2, 2022

Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3

FDA Devices Moderate Nov 2, 2022

Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 18mm Stem Base, REF 200252904, Size 4

FDA Devices Moderate Aug 31, 2022

Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.

FDA Devices Moderate Jul 20, 2022

Wright EVOLVE TRIAD Plate Cutter, REF 49510120

FDA Devices Moderate Jul 6, 2022

Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the INFINITY Total Ankle System.

FDA Devices Moderate Mar 9, 2022

The DARCO¿ Locking Bone Plate System is designed with rhombus (parallelogram) plates of biocompatible titanium. The plates use either 2.7mm or 3.5m…

FDA Devices Moderate Dec 29, 2021

Stryker DARCO Screw, Locking, Ti6A14V, REF DC2825016, 2.7mm x 16mm.

FDA Devices Moderate Dec 29, 2021

Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE Lisfranc Reconstruction System.

FDA Devices Moderate Dec 29, 2021

Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.

FDA Devices Moderate Dec 8, 2021

INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS

FDA Devices Moderate Sep 30, 2020

EVOLVE STEM 8.5MM Model # 496S085

FDA Devices Moderate Aug 19, 2020

Screw Removal Case Assembly, Part Number 1985BASE - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both …

FDA Devices Moderate May 13, 2020

WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left, REF 2000252902 - Product Usage: is intended to give a patient limited mobility by reducing pa…

FDA Devices Moderate Feb 12, 2020

WRIGHT EVOLVE Proline Head, Size: +2, OD: 20mm, REF 496H220

FDA Devices Moderate Feb 12, 2020

WRIGHT EVOLVE Proline Head, Size: +2, OD: 22mm, REF 496H222

FDA Devices Moderate Dec 4, 2019

PRO-STIM 10cc INJECTABLE, Part Number 86SR0410

FDA Devices Moderate Dec 4, 2019

Darco STERILE HEADED DRILL BIT 4.4MM , Part Number 777S06514

FDA Devices Moderate Dec 4, 2019

SWANSON FINGER JOINT #1, Part Number 4700001

FDA Devices Moderate Dec 4, 2019

INBONE STEM, TIBIAL, TOP, Part Number 200011901

FDA Devices Moderate Dec 4, 2019

CPS CALCANEAL PLATE SML 54MM, Part Number DCS2805001

FDA Devices Moderate Dec 4, 2019

EVANS OPENING WEDGE PLATE 10MM, Part Number 58S30010

FDA Devices Moderate Dec 4, 2019

SWANSON TRAPEZIUM IMPLANT, Part Number 4520002

FDA Devices Moderate Dec 4, 2019

SWANSON GREAT TOE, TITANIUM SZ 4, Part Number 4833104

FDA Devices Moderate Dec 4, 2019

VALOR SCREW 5.0MM X 45MM LEN, Part Number 4151150045

FDA Devices Moderate Sep 9, 2015

CrossCHECK Non-Locking Screw in the following sizes: 3.0 x 8 mm, REF CCP-N3008; 3.0 x 10 mm, REF CCP-N3010; 3.0 x 12 mm, REF CCP-N3012; 3.0 x 14 mm, …

FDA Devices Moderate Sep 9, 2015

CrossCHECK Locking Screw in the following sizes: 3.0 x 8 mm, REF CCP-L3008; 3.0 x 10 mm, REF CCP-L3010; 3.0 x 12 mm, REF CCP-L3012; 3.0 x 14 mm, RE…

FDA Devices Moderate May 27, 2015

PHALINX (TM) HAMMERTOE HANDLE, SIZE: LARGE, STYLE: ANGLED, REF 45304014, CONTENTS 1 EACH, RX ONLY

FDA Devices Moderate May 27, 2015

PHALINX (TM) HAMMERTOE HANDLE, SIZE: MEDIUM, STYLE: ANGLED, REF 45304013, CONTENTS 1 EACH, RX ONLY

FDA Devices Moderate May 27, 2015

PHALINX (TM) HAMMERTOE HANDLE, SIZE: X-SMALL, STYLE: ANGLED, REF 45304011, CONTENTS 1 EACH, RX ONLY

FDA Devices Moderate May 27, 2015

PHALINX (TM) HAMMERTOE HANDLE, SIZE: SMALL, STYLE: ANGLED, REF 45304012, CONTENTS 1 EACH, RX ONLY

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, MTP NX Plate, Left, Recon, REF CCP-MPN2L. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, LAPIDUS CX Plate, 1mm Step, Left, REF CCP-LPX1L. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, MTP CX Plate, Right, REF CCP-MPX1R. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, Utility Plate, 5-Hole, REF CCP-UTN5. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, MTP NX Plate, Right, Recon, REF CCP-MPN2R. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, HOCKEY STICK CX Plate, Right, REF CCP-HSX1R. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, Utility Plate, 6-Hole, REF CCP-UTN6. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, Utility Plate, 4-Hole, REF CCP-UTN4. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, Y-PLATE CX, REF CCP-YPX1. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, LAPIDUS CX Plate, NEUTRAL, Right, REF CCP-LPX0R. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, LAPIDUS CX Plate, 2mm Step, Left, REF CCP-LPX2L. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, MTP CX Plate, Left, REF CCP-MPX1L. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, LAPIDUS CX Plate, 1mm Step, Right, REF CCP-LPX1R. Orthopedic use.

FDA Devices Moderate Apr 29, 2015

CROSSCHECK(R) Plating system, LAPIDUS CX Plate, NEUTRAL, Left, REF CCP-LPX0L. Orthopedic use.

FDA Devices Moderate Sep 17, 2014

CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM, REF 40S20020, 1 EACH, Rx ONLY, NON STERILE Orthopedic

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds