International safety notice

Recall of one batch number of the product i-Visc 1.0, i-Medical Ophthalmic International GmbH

Germany / BfArM · DEU · Mar 14, 2014

Key facts

Title Recall of one batch number of the product i-Visc 1.0, i-Medical Ophthalmic International GmbH
Regulator Germany / BfArM
Country DEU
Brand Recall of one batch number of the product i-Visc 1.0, i-Medical Ophthalmic International GmbH
Manufacturer Recall of one batch number of the product i-Visc 1.0, i-Medical Ophthalmic International GmbH
Models 6221-75, 21-75, 701659, 21-750030-0, 6221-750030-0, 252078649, D-69123, 13M27
Date Mar 14, 2014
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

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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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