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Baxter Healthcare Corporation Recall 89823

Description: PrisMax System, Product Code 955724

Baxter Healthcare Corporation Recall 89823 Information

Mandated?Voluntary: Firm initiated
Recall NumberZ-0992-2022
Event ID89823
Event DescriptionPrisMax System, Product Code 955724
Product TypeDevices
DistributionWorldwide distribution - US Nationwide and the countries of Mexico, Brazil, Jamaica, Trinidad and Tobago, Canada, Australia, Singapore, Hong Kong, Vietnam, New Zealand, Korea, Austria, Belgium, Denmark, Estonia, Finland, France, Germany, Greece, Ireland, Israel, Italy, Luxemburg, Netherlands, Norway, Poland, Portugal, Saudi Arabia, Spain, Sweden, Switzerland, Turkey, and United Kingdom.
Quantity296 units
Recall ReasonThis correction is due to software anomalies occurring during use. If the operator initiates therapy by entering a value other than the default value for the patient Gain/Loss Limit or the Return Pressure Drop Limit (RDL) and uses the Same Patient function, the PrisMax System will return the patient Gain/Loss Limit or the RDL to the default value, rather than the non-default value entered at the initiation of treatment. The PrisMax System interface will display the original values once treatment is restarted but does not have an alert to inform the user of the change. The RDL value will be returned to the original value immediately upon selecting the Same Patient function. The Gain/Loss Limit value will be returned to the original value when the patient weight and/or hematocrit is changed during treatment.
Device Classification20220504
Device Code InfoGTIN 07332414126018, All Serial Numbers
Center Classification Date20220422
Recall Initiation Date20220315
Recalling FirmBaxter Healthcare Corporation
Initial Notification Letter
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