MicroPort Orthopedics recalls

MicroPort Orthopedics has 31 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 28 Jan 2026. 3 are still ongoing. 1 was reported in the last 12 months.

Total recalls31since 2014
Last 12 months1reported
Class I1445% of total
Ongoing3latest 28 Jan 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 14 45%Class II 11 35%Class III 6 19%

Why microport orthopedics is recalled

By year

Ongoing microport orthopedics recalls

3 active

All microport orthopedics recalls, newest first

31 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIMicroPort Hipturn Fem Head Trial Reusable recalledMicroPort OrthopedicsDevice Malfunction13 states
DeviceCLASS IIEvolution Mp Femoral Component Cs/cr Porous Size 5 Right Primary recalledMicroPort OrthopedicsPackaging DefectsTN
DeviceCLASS IIEvolution¿ MP Femoral CS/CR Non-Porous MicroPort total recalledMicroPort OrthopedicsPackaging DefectsTN
DeviceCLASS IIEvolution MP Tibial Bases, Size 2+ Left recalledMicroPort OrthopedicsPackaging DefectsTN
DeviceCLASS IIEvolution MP Tibial Bases, Size 7 Left recalled by MicroPort OrthopedicsMicroPort OrthopedicsPackaging DefectsTN
DeviceCLASS IIProfemur Plasma Z Classic Stem Size 7 Standard Short Neck recalledMicroPort OrthopedicsOtherNationwide
DeviceCLASS IProfemur Neck Extra Long Titanium recalled by MicroPort OrthopedicsMicroPort OrthopedicsOtherTN
DeviceCLASS IProfemur Neck Long Titanium recalled by MicroPort OrthopedicsMicroPort OrthopedicsOtherTN
DeviceCLASS IISchanz Screw Self Drill, Size recalled by MicroPort OrthopedicsMicroPort OrthopedicsSterilityNationwide
DeviceCLASS IIProfemur(r) R Rasp Handle recalled by MicroPort OrthopedicsMicroPort OrthopedicsOtherTN
DeviceCLASS IIILineage Liners recalled by MicroPort OrthopedicsMicroPort OrthopedicsForeign MaterialNationwide
DeviceCLASS IIILineage Shell recalled by MicroPort OrthopedicsMicroPort OrthopedicsForeign MaterialNationwide
DeviceCLASS IIIConserve Shells recalled by MicroPort OrthopedicsMicroPort OrthopedicsForeign MaterialNationwide
DeviceCLASS IIIConserve Cups recalled by MicroPort OrthopedicsMicroPort OrthopedicsForeign MaterialNationwide
DeviceCLASS IIIProcotyl (Rim- Lock) Liners recalled by MicroPort OrthopedicsMicroPort OrthopedicsForeign MaterialNationwide
DeviceCLASS IIIDynasty Liners recalled by MicroPort OrthopedicsMicroPort OrthopedicsForeign MaterialNationwide
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IAdvance(R) II Modular Tibial Base W/Screwholes, Knee Tibial Base recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IIProfemur(R) Modular Neck, Hip Femoral Neck MicroPort total recalledMicroPort OrthopedicsOtherTN
DeviceCLASS IProfemur Plus CoCr Modular Neck recalled by MicroPort OrthopedicsMicroPort OrthopedicsOtherNationwide
DeviceCLASS IIEvolution Mp Tibial Base recalled by Microport OrthopedicsMicroport OrthopedicsOther8 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.