International safety notice

Lot Recall of an infusion extension line named “T-connector Luer-Lock”, Hospira

Germany / BfArM · DEU · Sep 19, 2012

Key facts

Title Lot Recall of an infusion extension line named “T-connector Luer-Lock”, Hospira
Regulator Germany / BfArM
Country DEU
Brand Lot Recall of an infusion extension line named “T-connector Luer-Lock”, Hospira
Manufacturer Lot Recall of an infusion extension line named “T-connector Luer-Lock”, Hospira
Models 12-030-NY, Q.FA.EMEA.2012.012, OF8989701
Date Sep 19, 2012
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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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