Baxter recalls Prismaflex System and Control Unit for safety information on connector use. This recall addresses proper handling to prevent potential hazards.
Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.
Baxter is recalling its Prismaflex System and Control Unit due to safety information about proper connector use. This recall ensures users follow correct procedures to avoid risks.
The recall involves safety information from the operator's manual about connector use. Improper handling could lead to potential hazards if not followed correctly.
Users of the Prismaflex System and Control Unit are affected. Healthcare professionals using this medical device are most at risk.
Check for the product code 115269 or GTIN 07332414117702 on the Prismaflex System and Control Unit. This recall applies to devices sold by Baxter Healthcare Corporation.
Check the Prismaflex Operator's Manual for proper connector use instructions.
Baxter is communicating safety information from the Prismaflex Operator's Manual regarding proper connector use to prevent potential hazards.
Review the Prismaflex Operator's Manual for proper connector use instructions.
The recall addresses safety information to prevent potential hazards, but no specific injury risk is stated.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1831-2020 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1831-2020 from Baxter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
