Z-1775-2024 Class II Ongoing
FDA device recall Z-1775-2024 was initiated by Baxter Healthcare Corporation on Mar 20, 2024 and is designated Class II. Reason for recall: One device was improperly performed testing prior to release from a Service Center. The recall status is ongoing. Affected quantity: 1 pump.
Recall Details
- Product Type
- Devices
- Report Date
- May 15, 2024
- Initiation Date
- Mar 20, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1 pump
Product Description
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Reason for Recall
One device was improperly performed testing prior to release from a Service Center.
Distribution Pattern
US Nationwide distribution in the state of Massachusetts.
Code Information
UDI/DI 00085412610900, Serial Number 3540772
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1775-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026