PlainRecalls
FDA Devices Moderate Class II Terminated

Prismaflex System, Prismaflex Control Unit

Reported: May 6, 2020 Initiated: February 6, 2020 #Z-1832-2020

Product Description

Prismaflex System, Prismaflex Control Unit

Reason for Recall

Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.

Details

Units Affected
626
Distribution
Distribution in US, Puerto Rico
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Prismaflex System, Prismaflex Control Unit. Recalled by Baxter Healthcare Corporation. Units affected: 626.
Why was this product recalled?
Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 6, 2020. Severity: Moderate. Recall number: Z-1832-2020.