FDA Medical Device Recalls (openFDA)
NxStage Medical, Inc.: NxStage Express Fluid Warmer (FW-300, FW-300-A, FW-300-WW, FW-301, FW-301-A) Product Usage: The NxStage Express Fluid Warmer is an accessory to the NxStage System One used to warm therapy fluids prior to administration.
- Recall number
- Z-2793-2018
- Recalling firm
- NxStage Medical, Inc.
- Product
- NxStage Express Fluid Warmer (FW-300, FW-300-A, FW-300-WW, FW-301, FW-301-A) Product Usage: The NxStage Express Fluid Warmer is an accessory to the NxStage System One used to warm therapy fluids prior to administration.
- Status
- Terminated
- Initiated
- 2018-06-11
- Posted
- not on file
- Terminated
- 2020-04-28
- Reason
- There is a potential risk of electrical fire when fluid leaks into the power receptacle on the back of the warmer. The risk exists any time the warmer is plugged in. The firm has received 7 reports of smoke, sparks, or flames coming from the Express Fluid Warmer since 2016. No adverse events have been reported.
- Root cause
- Use error
- Action
- On June 11, 2018, the firm distributed Medical Device Product Safety Notices to affected customers and dialysis centers. Patients were contacted either via email or UPS second day air. Dialysis centers were contacted via email. The recall communication alerted customers that the firm has received 7 reports of smoke, sparks, or flames coming from the Express Fluid Warmer since 2016. No adverse health consequences or medical interventions have been reported. The firm informed customers that they were updating the User Guide to add the following new warning language: "Warning: Do not use any fluid bags that are leaking, and use caution not to spill fluids near the warmer. If the warmer is plugged in, leaking or spilled fluids in the warmer power receptacle can cause an electrical short even if the warmer is not being used. This can lead to an electrical fire and risk of serious injury or death. To minimize this risk, do the following: " When not used during treatment, do not plug the Express Fluid Warmer into the cycler. " Check all fluid bags for leaks prior to and during use. " If fluid spills onto the warmer, unplug the warmer power cord from the rear power receptacle and contact Technical Support." Customers were asked to do the following: 1. Please follow the instructions on the attached reply form to confirm that you received this notice. 2. Please observe the above warning and unplug your Express Fluid Warmer when not in use. If you have any questions or comments, please feel free to contact Customer Service at 1-800-NXSTAGE.
- Quantity
- 14975
- Distribution
- Worldwide Distribution - US Nationwide in the countries of Australia, Canada, France, Germany, Italy, Kuwait, Netherlands, Saudi Arabia, Spain, Sweden, and UK.
- Lot, serial or model codes
- All units are affected. As of 6/11/18, the last serial number manufactured was W35452.
- 510(k) numbers
- ["K071263"]
- PMA numbers
- not on file
- Product code
- KDI
- Firm FEI
- 3003464075
- Firm city
- Lawrence
- Firm state
- MA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28