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FDA (Device enforcement)Recalled 2023-12-22class i

Baxter Healthcare Corporation: Baxter Exactamix Pro 1200, REF EXM12DY

Hazard

An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant ingredient delivery of the requested overfill volume.

Details from the source

Reason for recall: An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant ingredient delivery of the requested overfill volume. Distribution: US: AL, AZ, CA, FL, GA, IA, KY, MD, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OR, SD, TX, WA, WI, Quantity: 8 devices Lot/code info: UDI/DI 05413765588150, Serial Numbers: PLD2314002, PLD2328001, PLD2328004, PLD2328042, PLD2314006, PLD2328002, PLD2328005, LD2339005

UPC codes

05413765588150

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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