International safety notice

Recall for Sterimedix/Altomed Ophthalmic Irrigation/Aspiration Coaxial Handpieces/Bimanual Handles, Sterimedix Ltd.

Germany / BfArM · DEU · Sep 27, 2010

Key facts

Title Recall for Sterimedix/Altomed Ophthalmic Irrigation/Aspiration Coaxial Handpieces/Bimanual Handles, Sterimedix Ltd.
Regulator Germany / BfArM
Country DEU
Brand Sterimedix/Altomed Ophthalmic Irrigation/Aspiration Coaxial Handpieces/Bimanual Handles, Sterimedix Ltd.
Manufacturer Recall for Sterimedix/Altomed Ophthalmic Irrigation/Aspiration Coaxial Handpieces/Bimanual Handles, Sterimedix Ltd.
Models 16876, 501491, 118483, 118517, 119073, M5510, 119087, M5501, 119069, 19091, M5584, M5513 and 9 more
Date Sep 27, 2010
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 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

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