International safety notice

Recall of one manufacturing lot of Procedure Pak called Ophthalmologie - Set I, Mölnlycke Health Care

Germany / BfArM · DEU · Oct 7, 2010

Key facts

Title Recall of one manufacturing lot of Procedure Pak called Ophthalmologie - Set I, Mölnlycke Health Care
Regulator Germany / BfArM
Country DEU
Brand Recall of one manufacturing lot of Procedure Pak called Ophthalmologie - Set I, Mölnlycke Health Care
Manufacturer Recall of one manufacturing lot of Procedure Pak called Ophthalmologie - Set I, Mölnlycke Health Care
Models 10341077, 83060241-07, 920214, 50031407
Date Oct 7, 2010
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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