FDAJanuary 29, 2018device

NxStage Dialysate Sack: 1) REF SAK-301 UDI-M535SAK3010, 2) REF SAK-302 UDI-M535SAK3020, 3) REF SAK-303 UDI-M535SAK3030, 4) REF SAK-304 UDI-M535SAK3040, 5) REF SAK-306 UDI-M535SAK3060, 6) REF SAK-307 UDI- M535SAK3070, 6) REF SAK-402 UDI-M535SAK4020, 7) REF SAK-405 UDI- M535SAK4050, 8) REF SAK-406 ...

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

The hazard

May contain endotoxin levels which have been confirmed to exceed the ANSI/AAMI quality standard dialysis fluid of 0.5 EU/ml when used to prepare product.

What to do

FDA enforcement status: Terminated

Brands named

nxstage medicalnxstage

Recall history

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

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