FDADecember 14, 2017device

2008 K2 Hemodialysis Machine with software version 5.40, Models: (1) Hemodialysis SYS OLC/Diasafe PLS 190610, UDI 00840861100859 (+Serial Number), (2) Machine Short Cap, OLC.DP HP 190630, UDI 00840861100866 (+Serial Number) ndicated for acute and chronic dialysis therapy.

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

The hazard

When the recirculation ultrafiltration (UF) Goal is set to a value greater than 200ml in service mode and the user starts a treatment using the SLED (Sustained Low Efficiency Dialysis) program the display will show an invalid message and the UF pump will run at the recirculation UF rate which may be up to 4000ml/hour. The SLED program is required to limit the UF rate to a maximum of 1000 ml/hour.

What to do

FDA enforcement status: Terminated

Brands named

fresenius medical care renal therapiesfreseniusfresenius medical

UPCs

0084086110085900840861100866

Recall history

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

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