# FDA recall Z-2262-2026 > **Baxter Healthcare Corporation** · Class II · device recall initiated 2026-04-22. ## Product Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector Valve) and a spike or other appropriate connector on the opposite end to attach the source container. ## Reason for recall 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. ## Distribution Worldwide - US Nationwide distribution including in the states of Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maine, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and West Virginia. The countries of Taiwan and Uruguay. ## Key facts - **Recall number:** Z-2262-2026 - **Recalling firm:** Baxter Healthcare Corporation - **Classification:** Class II - **Product type:** device - **Status:** Ongoing - **Initiation date:** 2026-04-22 - **Report date:** 2026-06-10 - **Voluntary/Mandated:** Voluntary: Firm initiated - **Location:** Deerfield, IL, United States ## Primary source FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2262-2026 ## Citation > MORVS. FDA recall Z-2262-2026. Retrieved 2026-10-22 from https://api.morvs.ai/recall/Z-2262-2026. Source: US FDA. Licensed CC0. --- *[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*