Recall Register

Food, drugs, devices › Firms

MicroPort Orthopedics Inc.

FDA recalling firm · 15 enforcement events · 33 product records · 2014–2025 · TN

MicroPort Orthopedics Inc. has 15 FDA enforcement events on this register (33 product records) between 2014 and 2025: 15 device; the busiest year was 2016 with 4.

20% of its events are Class I; the most common class is Class II (11). 4 events are listed as ongoing; the recalling firm's address is in TN.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
19 Dec 2025Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HTHT0036 Software Version: N/A Product Description: HIPTURN FEM HEAD TRIAL 36MM REUSABLEDeviceClass II1Ongoing
29 Oct 2024EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE 6 LEFT PRIMARY, REF: EFSRN6PL Knee prosthesis componentDeviceClass II1Ongoing
3 May 2024EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.DeviceClass II1Ongoing
28 Oct 2022EVOLUTION MP Tibial Bases, Size 2+ LEFT, REF ETPKN2PL, knee tibial baseDeviceClass II2Terminated
4 May 2022PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECKDeviceClass II1Terminated
31 Jul 2020PROFEMUR Neck Long Titanium, Catalog Numbers: PHA01204, PHA01214, PHA01224, PHA01234, PHA01244, PHA01254, PHA01264. Hip prosthesis component.DeviceClass I2Terminated
31 Jul 2020PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2 PHAC1202 PROFEMUR NECK NEUTRAL SHORT COBALT CHROME PHAC1204 PROFEMUR NECK NEUTRAL LONG COBALT CHROME PHAC1212 PROFEMUR NECK A/R VAR/VAL 2 SHORT COBALT CHROME PHAC1214 PROFEMUR NECK A/R VAR/VAL 2…DeviceClass II1Ongoing
18 Sep 2017MicroPort Orthopedics SCHANZ SCREW SELF DRILL, SIZE 4mm, REF 20070057, STERILE R Product Usage: MPO Total Hip Systems are indicated for use in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature patients with the following conditions: 1. non-inflammatory…DeviceClass II1Terminated
17 Nov 2016PROFEMUR(R) R RASP HANDLE, REF PPW38078, 1 EACH, NON-STERILE, MicroPort Orthopedics, Arlington, TN Instruments support the implantation of implants. Broach handles mate to the broach to allow for preparation of the femoral canal for the stem component to be implanted. ThisDeviceClass II1Terminated
30 Jun 2016PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK MicroPort total hip systems intended for use in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature patients.DeviceClass II1Terminated
21 Jun 2016Lineage Liners: REF 70102846, REF 70202852, REF 70202852, REF 70302858, REF 70303258, REF 70402864, REF 70403264, REF 70403664 For use with the conserve metal headDeviceClass III7Terminated
21 Jun 2016ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA10, SIZE 1 STD; SURFACE POROUS, HA COATED; FIT CEMENTLESS; USE W/ SIZE 1 FEMUR & SIZE 1 TIBIAL INSERT; CONTENTS, 1 EACH, STERILE R, Rx ONLY, MicroPort Knee Systems Total Knee Systems MicroPort Total Knee Systems are indicated for use in knee…DeviceClass I11Terminated
4 Aug 2015PROFEMUR PLUS CoCr MODULAR NECK, REF: PHAC1254, SIZE LONG, ORIENTATION 8 degree VAR/VAL. 12/14 SLT Taper. Orthopedic hip prosthesis component.DeviceClass I1Terminated
2 Feb 2015EVOLUTION MP TIBIAL BASE, REF ETPKN8SR, SIZE 8 RIGHT, TYPE PRIMARY, FIT CEMENTED, STYLE KEELED, STERILE R, Rx ONLY, MicroPort Orthopedics, Inc. Knee prosthesis component.DeviceClass II1Terminated
30 Apr 2014PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc. Orthopaedic surgical instrument.DeviceClass II1Terminated

By type and class

Device15
Class II11
Class I3
Class III1

Class I: 20% of this firm's events; 18% of all events on the register.

Events by year

14
16
18
20
22
24
26
Enforcement events for MicroPort Orthopedics Inc. by year initiated.

Questions and answers

How many FDA recalls has MicroPort Orthopedics Inc. had?

15 enforcement events (33 product records) on this register, 2014–2025: 15 device.

Are any MicroPort Orthopedics Inc. recalls ongoing?

4 events are listed as ongoing in the current openFDA export.

What class are MicroPort Orthopedics Inc. recalls?

11 Class II, 3 Class I, 1 Class III. 20% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.