Baxter Healthcare Corporation Recall 89823
Description: PrisMax System, Product Codes: a) 955558, b) 955627, c) 955701
Baxter Healthcare Corporation Recall 89823 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-0993-2022 |
| Event ID | 89823 |
| Event Description | PrisMax System, Product Codes: a) 955558, b) 955627, c) 955701 |
| Product Type | Devices |
| Distribution | Worldwide 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. |
| Quantity | 3513 units |
| Recall Reason | This 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 Classification | 20220504 |
| Device Code Info | a) 955558, UDI 07332414124359, b) 955627, UDI 07332414124700, c) 955701, UDI 07332414125844, All Serial Numbers |
| Center Classification Date | 20220422 |
| Recall Initiation Date | 20220315 |
| Recalling Firm | Baxter Healthcare Corporation |
| Initial Notification | Letter |
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