Z-1810-2024 Class II Ongoing
FDA device recall Z-1810-2024 was initiated by Baxter Healthcare Corporation on Apr 9, 2024 and is designated Class II. Reason for recall: There is a potential for cracks on the mount of the front panel of the device. The recall status is ongoing. Affected quantity: 9 units.
Recall Details
- Product Type
- Devices
- Report Date
- May 22, 2024
- Initiation Date
- Apr 9, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9 units
Product Description
Spectrum IQ Infusion pump, Product Code 357009
Reason for Recall
There is a potential for cracks on the mount of the front panel of the device.
Distribution Pattern
US Nationwide distribution in the states of Ohio, Wisconsin.
Code Information
UDI/DI 00085412610900, Serial Numbers: 3770692, 3770755, 3770781, 3770816, 3770932, 3771122, 3771364, 3771374, 3771419
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1810-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026