NxStage Medical, Inc.: 15 recalls on record

Recalls filed with 1 agency: FDA (15).

First recall on record: May 8, 2013. Most recent: June 26, 2024.

Risk classification: Class II: 15

Most recent recalls

DateAgencyProduct
June 26, 2024FDANxStage PureFlow-B Solution, Premixed Dialysate for Hemodialysis, Device Catalog Numbers …Z-2160-2024
December 25, 2019FDALow Volume Cartridge IFU (SKU CAR-125-B) used with the following devices: 1) NxStage O…Z-0697-2020
December 5, 2018FDANxStage PureFlow B Solution-RFP-402, Premixed Dialysate for Hemodialysis NxStage Pure…Z-0502-2019
December 5, 2018FDANxStage PureFlow B Solution-RFP-400, Premixed Dialysate for Hemodialysis. NxStage P…Z-0500-2019
December 2, 2015FDANxStage System One S Cycler (High Permeability Hemodialysis System) Model no. NX1000-5Z-0326-2016
July 2, 2014FDANxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-302 La…Z-1855-2014
July 2, 2014FDANxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-303 La…Z-1856-2014
July 2, 2014FDANxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-304 La…Z-1857-2014
July 2, 2014FDANxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-306 La…Z-1859-2014
July 2, 2014FDANxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-301 La…Z-1854-2014
July 2, 2014FDANxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-307 La…Z-1860-2014
July 2, 2014FDANxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-407 La…Z-1861-2014
July 2, 2014FDANxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-305 La…Z-1858-2014
March 5, 2014FDANxStage PureFlow-B Solution; Model/Catalog Number: RFP-401. Product is packaged in a cas…Z-1073-2014
May 8, 2013FDANxStage PureFlow-B Solution, Model/Catalog Number: RFP-401, packaged in a case The Nx…Z-1214-2013

Questions about this company

How many recalls does NxStage Medical, Inc. have?
Recalert has 15 U.S. recalls on record for NxStage Medical, Inc., published between May 8, 2013 and June 26, 2024.
What was the most recent NxStage Medical, Inc. recall?
FDA recall Z-2160-2024, published June 26, 2024: NxStage PureFlow-B Solution, Premixed Dialysate for Hemodialysis, Device Catalog Numbers RFP-400, RFP-401, RFP-402, RFP-403, RFP-404, RFP-405, RFP-406, RFP-453, RFP-454, RFP-456
Which agencies have handled NxStage Medical, Inc. recalls?
NxStage Medical, Inc. appears as the recalling firm in recalls from: FDA (15).

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