International safety notice

It is possible that a product was discovered overseas where the size of the packaged product differs from the label on the product box, and this may have affected the product. We have decided to voluntarily recall a certain product.

Japan / PMDA Recalls · JPN · Nov 7, 2022

Key facts

Title It is possible that a product was discovered overseas where the size of the packaged product differs from the label on the product box, and this may have affected the product. We have decided to voluntarily recall a certain product.
Regulator Japan / PMDA Recalls
Country JPN
Brand Common name: total knee prosthesis Brand name: EVOLUTION MP artificial knee joint system
Manufacturer Microport Orthopedics Japan Co., Ltd.
Models 1916559, ETPKN2PL
Date Nov 7, 2022
Regulator page info.pmda.go.jp

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices