FDA recall record

MicroPort Orthopedics PROFEMUR Neck Long Titanium, Catalog Numbers: PHA01204, PHA01214 recall — FDA Z-2941-2020

MicroPort Orthopedics Inc. states that there have been reports of fractures of the long and extra-long Titanium modular femoral neck component after…

Class Iclassification
Z-2941-2020official record ID
Sep 30, 2020report date

Recall record at a glance

Official recordZ-2941-2020
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMicroPort Orthopedics Inc.
Report dateSep 30, 2020
Recall initiation dateJul 31, 2020
Quantity123,284 units
LocationArlington, TN, United States

Official product description

PROFEMUR Neck Long Titanium, Catalog Numbers: PHA01204, PHA01214, PHA01224, PHA01234, PHA01244, PHA01254, PHA01264. Hip prosthesis component.

Why the product was recalled

MicroPort Orthopedics Inc. states that there have been reports of fractures of the long and extra-long Titanium modular femoral neck component after implantation. Worldwide there were 680 Long and X-Long PROFEMUR Titanium modular neck fractures among 123,840 global sales representing is a cumulative rate of modular neck device fracture of 0.55% from 2002 to 2019. Within the United States there were 349 Long and X-Long PROFEMUR Titanium modular neck fractures among 15,786 United States sales representing a cumulative rate of modular neck device fracture with a fracture rate in the United States of 2.21% from 2002 to 2019. There is an average time of 5.4 years to device fracture after implantation.

Distribution information

worldwide, except China and Japan

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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