PlainRecalls

Wright Medical Technology, Inc.

Compiled from official public sources by the publisher.

78 recalls on record · Latest: Apr 10, 2024

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Agency notice ledger

Federal filing book Wright Medical Technology,… MID-BOOK · SINGLE-AGENCY

#234 of 14,151 · 78 notices · 0.075% archive

  • BOOK 78 notices
  • RANK #234 of 14,151
  • SHARE 0.075% archive
  • AGENCY FDA Devices (78)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 10, 2024
  • PHOTO Angiodynamics Inc.

Nearest notice-volume peer: Angiodynamics Inc. (Navilyst Medical Inc.) (0 notice gap)

Wright Medical Technology, Inc. accounts for about 0.075% of the 104,423-notice archive on 78 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Wright Medical Technology,… compares to 14,151 recalling firms

Wright Medical Technology, Inc. ranks 234th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Wright Medical Technology,… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

78 234th of 14151 higher than 13,917 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Wright Medical Technology,… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Wright Medical Technology, Inc. holds about 0.075% of archive notices alongside 78 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
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 Mar 8, 2023

ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, 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 Oct 12, 2022

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 radial head fractures. It combines parts of two systems: EVOLVE Proline and EVOLVE TRIAD.
FDA Devices Moderate Oct 12, 2022

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 head fractures. It combines parts of two systems: EVOLVE Proline and EVOLVE TRIAD.
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 Apr 6, 2022

EasyFuse Dynamic Compression System Instrument Pack
FDA Devices Moderate Mar 23, 2022

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.
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 3.5mm screws which intersect each other in pairs. The drill holes of the plates are aligned to assure the screws do not touch. The various plates model numbers differ from each other through among other things different curvatures, material strengths, lengths, number of plate holes and through different grades and bridge widths
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 Dec 8, 2021

INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm 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 plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles and a range of k-wires to assist in removal of cannulated screws. This product is a multiple use, non-sterile instrument.
FDA Devices Moderate Aug 19, 2020

Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles and a range of k-wires to assist in removal of cannulated screws. This product is a multiple use, non-sterile instrument.
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 pain, restoring alignment and replacing the flexion and extension movement in the ankle joint.
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 Dec 4, 2019

Dart Fire HEADED SCREW 4.0X 32MM, Part Number D1S40032S
FDA Devices Moderate Dec 4, 2019

ORTHOLOC 3DI PLT SYS STERILE, LOCKING SCREW, 3.5 x 38mm Sterile, Part Number 58S03538
FDA Devices Moderate Dec 4, 2019

SWANSON FINGER JOINT #2, Part Number 4700002
FDA Devices Moderate Apr 25, 2018

WRIGHT, Wright Medical Technology, VALOR(R) Nail, Right, Medium, OD: 10mm, L: 200mm, REF415101020
FDA Devices Moderate Apr 25, 2018

WRIGHT, Wright Medical Technology, VALOR(R) Nail, Right, Small, OD: 11.5mm, L: 150mm, REF415101115R
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, REF CCP-N3014l; 3.0 x 16 mm, REF CCP-N3016; 3.0 x 18 mm, REF CCP-N3018; 3.0 x 20 mm, REF CCP-N3020; 3.0 x 22 mm, REF CCP-N3022; 3.0 x 24 mm, REF CCP-N3024; 3.0 x 26 mm, REF CCP-N3026; 3.0 x 28 mm, REF CCP-N3028; 3.0 x 30 mm, REF CCP-N3030; 3.0 x 32 mm, REF CCP-N3032; 3.0 x 34 mm, REF CCP-N3034; 3.0 x 36 mm, REF CCP-N3036; 3.0 x 38 mm, REF CCP-N3038;
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, REF CCP-L3014; 3.0 x 16 mm, REF CCP-L3016; 3.0 x 18 mm, REF CCP-L3018; 3.0 x 20 mm, REF CCP-L3020; 3.0 x 22 mm, REF CCP-L3022; 3.0 x 24 mm, REF CCP-L3024; 3.0 x 26 mm, REF CCP-L3026; 3.0 x 28 mm, REF CCP-L3028; 3.0 x 30 mm, REF CCP-L3030; 3.0 x 32 mm, REF CCP-L3032; 3.0 x 34mm, REF CCP-L3034; 3.0 x 36 mm, REF CCP-L3036; 3.0 x 38 mm, REF CCP-L3038; 3.0
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.

Wright Medical Technology,… carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Angiodynamics Inc. (Navilyst Medical Inc.) 78 Draeger Medical, Inc. 78 Abiomed, Inc. 79 Philips Medical Systems Nederlands 79

Frequently Asked Questions

How many federal recall notices name Wright Medical Technology,…? ▼
PlainRecalls indexes 78 distinct federal recall events naming Wright Medical Technology, Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Wright Medical Technology,… sit among other recalling firms? ▼
Wright Medical Technology, Inc. ranks #234 of 14,151 by distinct recall-event count among 14,151 firms in this archive (98th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Wright Medical Technology,…'s notices? ▼
FDA Devices accounts for 78 of this firm's 78 indexed notices.
What product category dominates Wright Medical Technology,…'s filing book? ▼
Filings for Wright Medical Technology, Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Wright Medical Technology, Inc.: 78 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Wright Medical Technology, Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026