International safety notice

Cabeza femoral Biolox® Delta Ceramic V40™. Ver referencias y números de lote afectados en la nota de aviso de la empresa.

Spain / AEMPS · ESP · Feb 14, 2022

Key facts

Title Cabeza femoral Biolox® Delta Ceramic V40™. Ver referencias y números de lote afectados en la nota de aviso de la empresa.
Regulator Spain / AEMPS
Country ESP
Brand Cabeza femoral Biolox® Delta Ceramic V40™. Ver referencias y números de lote afectados en la nota de aviso de la empresa.
Manufacturer Stryker Joint Replacement, EEUU
Models 2.12-1, 28108, 89549404, 6570-0-232, RA2022-2911584, 04546540608536, 2022-060, 89546202, 76362, 04546540608475, 28022, 89648805 and 9 more
Event type Safety Notice
Date Feb 14, 2022

At a glance

  • No Recall
  • Yes 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