Profemur Cobalt Chrome Modular Neck Hip Replacements: Higher Than Anticipated Risk Of Revision Surgery, Metal-wear Effects And Component Fracture (dsi/2025/005)

Profemur cobalt chrome modular neck hip replacement components are being recalled in the UK because they show higher than expected rates of wear, corrosion, and fracture, leading to more patients needing revision surgery. The UK's MHRA medical device regulator identified these risks through an investigation. This affects people in the UK who have received these specific hip replacement components.

Recalling firm
Higher than anticipated risk of revision surgery
Reason
An MHRA investigation has found increased risks of wear and corrosion, including an increased occurrence of device fracture and revision surgery associated with cobalt chrome-containing Profemur modular neck hip stem components.
Classification
Unclassified
Category
drug recall
Country
United Kingdom
Agency
UK Medicines and Healthcare products Regulatory Agency
Recall date
2025-09-04
Status
Ongoing
Distribution
United Kingdom

Official recall notice from UK Medicines and Healthcare products Regulatory Agency

Recall details on Nibble Recalls: https://trynibble.app/recalls/ab4ff54a-04be-481f-8554-1f2dcfb85dfb