International safety notice

Indiana Ophthalmics

United Kingdom / MHRA · GBR · Nov 22, 2023

Key facts

Title Indiana Ophthalmics
Regulator United Kingdom / MHRA
Country GBR
Brand AACARB, AACOMER, PUROPTICS
Manufacturer Indiana Ophthalmics
Models 441277286199, 447859809049, QA2.INDIANA, 447791913552, 912752243939, 249-ONGAR, 912752241554
Event type Recall, Safety Notice
Action type Field safety notice
Date Nov 22, 2023
Regulator page gov.uk

At a glance

  • Yes Recall
  • Yes Field safety notice

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

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