FDA recall record

NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-301 Lactate recall — FDA Z-1854-2014

SAK Dialysate Concentrate contain aluminum levels which exceed internal product specification

Class IIclassification
Z-1854-2014official record ID
Jul 2, 2014report date

Recall record at a glance

Official recordZ-1854-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNxStage Medical, Inc.
Report dateJul 2, 2014
Recall initiation dateMay 14, 2014
Quantity13474 cases
LocationLawrence, MA, United States

Official product description

NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-301 Lactate 45, Potassium 1, Sodium 140, Calcium 3, Magnesium 1, Chloride 100, Glucose (mg/dL) 100 Batch Size (liters) 60 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.

Why the product was recalled

SAK Dialysate Concentrate contain aluminum levels which exceed internal product specification

Distribution information

Worldwide Distribution - USA (nationwide) and Internationally to France, Netherlands, Spain, Sweden, and the UK.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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