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Infusion Pump Recall: Zyno Medical Removes Certain Z-800, Z-800F, Z-800W, and Z800WF Infusion Pumps due to an Air-in-Line Software Defect That May Allow Larger than Expected Air Bubbles to Enter Patients
Nevada Medicaid·NV·Provider Announcement
Effective date
Nov 1, 2024
We identified it
Jun 21, 2026
Summary
Zyno Medical has issued a Class I recall (most serious type) for certain Z-800 series infusion pumps due to a software defect that may allow dangerous air bubbles to enter patients. Healthcare facilities must immediately stop using these recalled devices as they may cause serious injury or death.
Action Required
Immediately: Clinical staff must identify and remove all Zyno Medical Z-800, Z-800F, Z-800W, and Z-800WF infusion pumps from service. Contact Zyno Medical local business partner or email feedback@intuvie.com for recall instructions. Review FDA recall notice for specific device serial numbers and next steps. Continued use may cause serious patient injury or death.