Baxter Healthcare recalls Exacta Mix Vented Micro-Volume Inlet model H938175 with incorrect 0.8-micron filters that may cause incomplete or slower transfers of ingredients, leading to clinical effects like electrolyte imbalance.
Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow efficiency, incomplete or slower transfers of ingredients, or system alarms. This issue may lead to clinical effects such as electrolyte imbalance, metabolic instability, delayed recovery, etc.
Baxter Healthcare is recalling Exacta Mix Vented Micro-Volume Inlet tubing sets with model number H938175 due to potential incorrect 0.8-micron filters. This could cause incomplete or slower transfers of ingredients, potentially leading to clinical effects such as electrolyte imbalance or metabolic instability.
The tubing sets may contain 0.8-micron filters instead of the required 3-micron filters. This can reduce flow efficiency, cause incomplete or slower transfers of ingredients, and potentially lead to clinical effects like electrolyte imbalance or metabolic instability.
Healthcare professionals using Exacta Mix Vented Micro-Volume Inlet tubing sets with model H938175. Patients receiving treatments through these devices may be at risk of electrolyte imbalance or metabolic instability.
Check for model number H938175 on the tubing sets. Affected lots include 804084, 804088, and 804089. The UDI number is 00085412475806.
Verify that the filter is a validated 3-micron filter, not a 0.8-micron filter.
The model number is H938175.
Lots 804084, 804088, and 804089 are affected.
Using a 0.8-micron filter instead of the validated 3-micron filter may cause incomplete or slower transfers of ingredients, potentially leading to clinical effects like electrolyte imbalance or metabolic instability.
We’ve drafted a message you can send Exacta Mix to request your refund or repair — edit it as you like.
Subject: Recall Z-2262-2026 — Exacta Mix Exacta Mix Hello, I own a Exacta Mix that is covered by recall Z-2262-2026 from Exacta Mix. 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.
