Recall Register

Wright Medical Technology, Inc.: FDA recalls

FDA enforcement reports name Wright Medical Technology, Inc. as the recalling firm in 26 events. The events have 78 product records. The recalls started from 2012 to 2024. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

26 events, newest first.

FDA enforcement events of Wright Medical Technology, Inc.
InitiatedProduct (first record)TypeClassRecordsStatus
6 Mar 2024stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplastyDeviceClass II1Ongoing
13 Jun 2023Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.DeviceClass II1Ongoing
10 Apr 2023stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixationDeviceClass II2Ongoing
2 Feb 2023ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone fixation deviceDeviceClass II2Ongoing
30 Sep 2022Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3DeviceClass II2Terminated
3 Aug 2022stryker 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.DeviceClass II2Ongoing
27 Jul 2022Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.DeviceClass II1Ongoing
14 Jun 2022Wright EVOLVE TRIAD Plate Cutter, REF 49510120DeviceClass II1Ongoing
2 Jun 2022Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the INFINITY Total Ankle System.DeviceClass II1Ongoing
10 Mar 2022EasyFuse Dynamic Compression System Instrument PackDeviceClass II1Terminated
15 Feb 2022Wright 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.DeviceClass II1Terminated
9 Feb 2022The 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…DeviceClass II1Terminated
3 Dec 2021Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.DeviceClass II2Ongoing
3 Dec 2021Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE Lisfranc Reconstruction System.DeviceClass II1Ongoing
4 Nov 2021INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUSDeviceClass II2Terminated
26 Aug 2020EVOLVE STEM 8.5MM Model # 496S085DeviceClass II1Terminated
28 Jul 2020Hardware 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…DeviceClass II2Terminated
9 Apr 2020WRIGHT 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.DeviceClass II1Terminated
27 Dec 2019WRIGHT EVOLVE Proline Head, Size: +2, OD: 20mm, REF 496H220DeviceClass II2Terminated
14 Mar 2018WRIGHT, Wright Medical Technology, VALOR(R) Nail, Right, Medium, OD: 10mm, L: 200mm, REF415101020DeviceClass II2Terminated
8 Nov 2016SWANSON GREAT TOE, TITANIUM SZ 4, Part Number 4833104DeviceClass II12Terminated
21 Jul 2015CrossCHECK 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…DeviceClass II2Terminated
16 Apr 2015PHALINX (TM) HAMMERTOE HANDLE, SIZE: X-SMALL, STYLE: ANGLED, REF 45304011, CONTENTS 1 EACH, RX ONLYDeviceClass II4Terminated
6 Mar 2015CROSSCHECK(R) Plating system, HOCKEY STICK CX Plate, Left, REF CCP-HSX1L. Orthopedic use.DeviceClass II19Terminated
30 Jul 2014CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM, REF 40S20020, 1 EACH, Rx ONLY, NON STERILE OrthopedicDeviceClass II9Terminated
5 Sep 2012Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28, OT22C58, Lot Numbers: W07335080 and X06391225 INSERT MOBILE "COLLEGIA" TAILLE 60*28, OT22C60, Lot Number: X06391226 TETE INOX "COLLEGIA" T 28/0 CONE 6 DEG. -N30NW-, OT32H28, Lot Numbers: 068573172 and X03396534 PROFEMUR(R) Z FEMORAL STEM S 1 CEMENT LESS,…DeviceClass II3Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Wright Medical Technology, Inc.: events for each product type
TypeEvents
Device26
Wright Medical Technology, Inc.: events in each class
ClassEvents
Class II26
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
10

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Wright Medical Technology, Inc., by the year that the recall started. The largest year is 2022, with 8 events.

Official channels

Cite this page

Recall Register. Wright Medical Technology, Inc.: FDA recalls. https://recallregister.com/firm/wright-medical-technology-inc/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
TN

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Wright Medical Technology, Inc. have?
Class II: 26 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Wright Medical Technology, Inc.?
FDA event 94194, which the firm started on 6 Mar 2024. The first product in the record is: stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
How many FDA recalls of Wright Medical Technology, Inc. have the status Ongoing?
10 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.