Baxter Spectrum IQ Infusion Pump, Product Code 3570009
This recall is currently active, issued May 3, 2024. It was issued by Baxter Healthcare Corporation.
- Company
- Baxter Healthcare Corporation
- Recall Initiated
- March 20, 2024
- Posted
- May 3, 2024
- Recall Number
- Z-1775-2024
- Quantity
- 1 pump
- Firm Location
- Deerfield, IL
- Official Source
- View on FDA website ↗
Reason for Recall
One device was improperly performed testing prior to release from a Service Center.
Distribution
US Nationwide distribution in the state of Massachusetts.
Lot / Code Info
UDI/DI 00085412610900, Serial Number 3540772
Root Cause
Nonconforming Material/Component
Action Taken
The affected customer was contacted via on-site visit on March 20, 2024, and by phone call on March 22, 2024. Baxter has asked the customer to locate the affected pump at their facility and return the device to Baxter for testing.
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