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. The most frequent reason is sterility.

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

0Oct '24 0 1 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 1Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

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

Why microport orthopedics is recalled

Product types

By year

202613%
202426%
202326%
202213%
202026%
201726%
20161858%
201526%
201413%

Ongoing microport orthopedics recalls

3 active

Reported	Class	Recall	Company	Reason	Where
28 Jan 2026Device	CLASS II	MicroPort Hipturn Fem Head Trial Reusable recalled	MicroPort Orthopedics	Device Malfunction	13 states
25 Dec 2024Device	CLASS II	Evolution Mp Femoral Component Cs/cr Porous Size 5 Right Primary recalled	MicroPort Orthopedics	Packaging Defects	TN
10 Jul 2024Device	CLASS II	Evolution¿ MP Femoral CS/CR Non-Porous Non-porous recalled	MicroPort Orthopedics	Packaging Defects	Nationwide

All microport orthopedics recalls, newest first

31 total

Reported	Class	Recall	Company	Reason	Where
28 Jan 2026Device	CLASS II	MicroPort Hipturn Fem Head Trial Reusable recalled	MicroPort Orthopedics	Device Malfunction	13 states
25 Dec 2024Device	CLASS II	Evolution Mp Femoral Component Cs/cr Porous Size 5 Right Primary recalled	MicroPort Orthopedics	Packaging Defects	TN
10 Jul 2024Device	CLASS II	Evolution¿ MP Femoral CS/CR Non-Porous Non-porous recalled	MicroPort Orthopedics	Packaging Defects	Nationwide
22 Feb 2023Device	CLASS II	Evolution MP Tibial Bases, Size 2+ Left recalled	MicroPort Orthopedics	Packaging Defects	Nationwide
22 Feb 2023Device	CLASS II	Evolution MP Tibial Bases, Size 7 Left recalled by MicroPort Orthopedics	MicroPort Orthopedics	Packaging Defects	Nationwide
8 Jun 2022Device	CLASS II	Profemur Plasma Z Classic Stem Size 7 Standard Short Neck recalled	MicroPort Orthopedics	Other	Nationwide
30 Sep 2020Device	CLASS I	Profemur Neck Extra Long Titanium recalled by MicroPort Orthopedics	MicroPort Orthopedics	Other	TN
30 Sep 2020Device	CLASS I	Profemur Neck Long Titanium recalled by MicroPort Orthopedics	MicroPort Orthopedics	Other	TN
1 Nov 2017Device	CLASS II	Schanz Screw Self Drill, Size recalled by MicroPort Orthopedics	MicroPort Orthopedics	Lead & Heavy Metals	Nationwide
11 Jan 2017Device	CLASS II	Profemur(r) R Rasp Handle recalled by MicroPort Orthopedics	MicroPort Orthopedics	Sterility	TN

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.