FDAOctober 5, 2017device

2008T, Hemodialysis Delivery System Product Indicated for acute and chronic dialysis therapy.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

While reviewing documentation for the next software release of the 2008T, an R&D technician identified that setting the UF goal to '0' introduces a discrepancy between the UF rate displayed and the actual UF pump rate. The software anomaly is also applicable to the 2008T Machines that contained the 2.63 Bug Fix per DCAF 17-088. 2008T Upgrade kits that contained the 2.63 Bug Fix are also affected. Additionally, SW version 2.64 (in design freeze) is also impacted by this anomaly.

What to do

FDA enforcement status: Terminated

Brands named

fresenius medical care renal therapiesfreseniusfresenius medical

UPCs

0084086110091000840861100927

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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2008T, Hemodialysis Delivery System Product Indicated for acute and chronic dialysis therapy. — Recall Details · AllClear