FDADecember 21, 2017device
MARS Treatment Kit, Use only with MARS(R) Monitor 1TC, GAMBRO, Product Code 800541
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Baxter has received customer complaints regarding leakage in the albumin circuit. The leakage was caused by an inadequate adhesive connection of the tubing to the Hansen connector of the MARS Tube Set which is part of the MARS Treatment Kit.
What to do
FDA enforcement status: Terminated
Brands named
baxter healthcarebaxter
UPCs
37332414107728
Recall history
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