Data Foundry

Medical device recalls 2014

NxStage Dialysate Sack — Class II medical device recall Z-1859-2014

Terminated recall by NxStage Medical, Inc., reported 2014-07-02, distributed nationwide. SAK Dialysate Concentrate contain aluminum levels which exceed internal product specification

Recall numberZ-1859-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmNxStage Medical, Inc., Lawrence, MA, United States
Recall initiated2014-05-14
Classified2014-06-24
Reported by FDA2014-07-02
Terminated2017-03-13
DistributedNationwide (US)
Countries outside the USES, FR, GB, NL, SE
Quantity2,711 cases
Lot numbers3047916, 3047917, 31279092
Model numbersSAK-306

Product

NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-306 Lactate 45, Potassium 2, Sodium 140, Calcium 3, Magnesium 1, Chloride 101, Glucose (mg/dL) 100 Batch Size (liters) 50 The SAK is one of the disposables used with NxStage PureFlow SL Dialysate Preparation System. The SAK is a disposable bag pre-filled with dialysate concentrate that is then filled with purified water prepared by NxStage PureFlow SL Dialysate Preparation System to prepare a batch of dialysate for use with the NxStage System One. SAKs are packaged in a case containing two SAKs. SAK product SKUs vary in the dialysate concentrate and volume of the final dialysate batch.

Reason for recall

SAK Dialysate Concentrate contain aluminum levels which exceed internal product specification

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1859-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.