Zyno Medical recalls Z-800 infusion systems with model numbers Z-800, Z-800F, Z-800W, Z-800WF due to potential battery depletion from self-discharge and parasitic leakage current even when plugged in. Affected units include specific lot codes.
Potential for the battery to deplete over time from self-discharge and internal parasitic leakage current despite being continuously plugged into AC mains.
Zyno Medical is recalling its Z-800 infusion systems (models Z-800, Z-800F, Z-800W, Z-800WF) because the battery may deplete over time even when plugged into an AC power source. This could lead to interrupted treatment if the system stops working unexpectedly during medical use.
The battery in these infusion systems can deplete due to self-discharge and internal parasitic leakage current, even when continuously connected to an AC power source. This means the system might stop working unexpectedly during medical treatment without warning.
Healthcare professionals using the Z-800 infusion system for intravenous treatments are most at risk. Patients receiving care with these devices may experience treatment interruptions if the system fails.
Check for model numbers Z-800, Z-800F, Z-800W, or Z-800WF on the device. Affected units include specific lot codes listed in the recall notice.
Identify the model number on your Z-800 infusion system to confirm if it is affected.
Reach out to Zyno Medical for guidance on next steps if your device is affected.
The battery may deplete over time due to self-discharge and internal parasitic leakage current, even when plugged into an AC power source.
Models Z-800, Z-800F, Z-800W, and Z-800WF.
No. The recall is for potential battery depletion, which is a low-risk issue that does not require immediate discontinuation of use.
We’ve drafted a message you can send Zyno Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0506-2025 — Zyno Medical Zyno Medical Hello, I own a Zyno Medical that is covered by recall Z-0506-2025 from Zyno Medical. 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.