NxStage recalls Express Fluid Warmers (FW-300 series) due to potential electrical fire if fluid leaks into power receptacle. No injuries reported but 7 smoke/sparks incidents since 2016.
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.
NxStage is recalling its Express Fluid Warmers (FW-300, FW-301 models) because fluid leaks could cause electrical fires when plugged in. This risk exists even with the device turned off, though no injuries have been reported.
Fluid leaks into the power port on the back of the warmer can cause electrical arcing, leading to sparks or flames. This risk occurs whenever the device is plugged in, even when not in use.
Healthcare facilities using the NxStage Express Fluid Warmer for medical fluid warming are most at risk. Patients receiving warmed fluids through this device could be affected.
Check for models labeled FW-300, FW-300-A, FW-300-WW, FW-301, or FW-301-A. The device is used with NxStage System One for warming medical fluids. All units are affected as of June 11, 2018.
Identify your warmer's model number on the label or packaging to confirm if it's in the recalled series (FW-300, FW-300-A, FW-300-WW, FW-301, FW-301-A).
Immediately unplug the warmer from the power source to prevent electrical hazards if fluid leaks occur.
Yes, if you use the NxStage Express Fluid Warmer for medical fluid warming, your device is affected as all models are recalled.
The recall includes all units manufactured up to June 11, 2018, with the last serial number W35452.
No adverse events have been reported, though 7 incidents of smoke, sparks, or flames occurred since 2016.
We’ve drafted a message you can send NxStage to request your refund or repair — edit it as you like.
Subject: Recall Z-2793-2018 — NxStage NxStage Hello, I own a NxStage that is covered by recall Z-2793-2018 from NxStage. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
