Edwards Lifesciences recalls EV1000A, EV1000NI, and EV1000CS monitors for potential fire risk from liquid entering AC power outlets. Affected units may need replacement.
Potential for an electrical short circuit leading to possible fire hazard due to liquid ingress into AC power outlets.
Edwards Lifesciences is recalling three models of EV1000 Clinical Platform monitors because liquid can enter the AC power outlets, causing a short circuit and possible fire. This could lead to serious injury or property damage if the device is used without proper precautions.
Liquid can enter the AC power outlets of the monitor, causing an electrical short circuit. This short circuit may lead to a fire hazard, especially if the device is used in environments where moisture is present.
Healthcare professionals using the EV1000A monitor for fluid management are most at risk. Patients receiving care with these monitors may also be affected.
Check for the model numbers EV1000A, EV1000NI, or EV1000CS on the monitor. These devices were sold for clinical use to optimize fluid management.
Inspect the AC power outlets for signs of liquid damage or corrosion.
Reach out to Edwards Lifesciences for guidance on next steps if liquid ingress is found.
No, this recall applies only to clinical use in healthcare settings.
Check for model numbers EV1000A, EV1000NI, or EV1000CS on the monitor, which are used for clinical fluid management.
Contact Edwards Lifesciences for guidance on next steps if liquid ingress is found.
We’ve drafted a message you can send Edwards Lifesciences to request your refund or repair — edit it as you like.
Subject: Recall Z-1193-2019 — Edwards Lifesciences Edwards Lifesciences Hello, I own a Edwards Lifesciences that is covered by recall Z-1193-2019 from Edwards Lifesciences. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
