US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of water to be used for hemodialysis Vivonic Part Numbers: G02020110 Fresenius Part Number: 24-090A-1
FDA Recall Z-2141-2024 · Posted 2024-06-13
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Recalling FirmFresenius Medical Care Holdings, Inc.
Recall StatusOpen, Classified
Product CodeFIP
Date Initiated2024-05-16
Product Quantity4 units
Reason for Recall
Concentrate Flow was exceeding the maximum 19.9 bar set point. The standard default set point range is between 4 and 18.Error message (F020104, "concentrate pressure alarm limit exceeded") concentrate pressure is too high and stops the dialysis water supply.
Firm Action
Fresenius Medical issued Urgent Medical Device Correction letter on 5-16-2024.
Letter states reason for recall, health risk and action to take:
A Fresenius Medical Care Water Systems Service Specialist will be contacting you to schedule an evaluation of your Water Treatment system and provide feedback on your system. For questions or concerns, please contact Fresenius Medical Care Technical Services at 800-227-2572, OPTION 4.
" Please provide this letter to your Biomedical Technician
" Report any complaints or adverse events to [email protected] or FDA MedWatchathttps://www.fda.gov/safety/medical-product-safety-information/medwatch-forms-fda-safety-reporting.
" Provide this Customer Notice to all those who need to be aware within your organization.
" Complete and return the attached reply form.
Root Cause
Process control
Distribution Pattern
US Nationwide distribution in the states of AL, IN, AK, WI.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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