SPECTRUM Pump, Model No. 35700BAX. Intended to be used for the controlled administration of intravenous fluids.
Reported: October 8, 2014 Initiated: September 3, 2014 #Z-2738-2014
Product Description
SPECTRUM Pump, Model No. 35700BAX. Intended to be used for the controlled administration of intravenous fluids.
Reason for Recall
One Service Technician may not have correctly serviced specific Sigma Spectrum Infusion Pumps according to established procedures during the time period of 5/5/2014 through 6/3/2014.
Details
- Recalling Firm
- Baxter Healthcare Corp.
- Units Affected
- USA: 56 units, Canada: 2 units
- Distribution
- Worldwide Distribution -- USA and Canada.
- Location
- Round Lake, IL
Frequently Asked Questions
What product was recalled? ▼
SPECTRUM Pump, Model No. 35700BAX. Intended to be used for the controlled administration of intravenous fluids.. Recalled by Baxter Healthcare Corp.. Units affected: USA: 56 units, Canada: 2 units.
Why was this product recalled? ▼
One Service Technician may not have correctly serviced specific Sigma Spectrum Infusion Pumps according to established procedures during the time period of 5/5/2014 through 6/3/2014.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 8, 2014. Severity: Moderate. Recall number: Z-2738-2014.
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