FDAAugust 24, 2016device
Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an Intravascular Administration Set for the administration or withdrawal of fluids to a patient through ...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
ICU Medical Inc. has identified a potential risk of leaking with certain Tego Connector devices.
What to do
FDA enforcement status: Terminated
Brands named
icu medicalicu
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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