Lower riskMedical device recall · FDA · Published April 22, 2026
Exacta Mix Vented Micro-Volume Inlet Recall: Incorrect Filter May Cause Incomplete
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.
Take action
Contact the company
📍Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy · Deerfield, IL 60015-4625
✎ GovInfoNow plain-language explainer
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. Read more at govinfonow.com/recall/49404-exacta-mix-vented-micro-volume-inlet-recall-incorrect-filter-may.
“Exacta Mix Vented Micro-Volume Inlet Recall: Incorrect Filter May Cause Incomplete.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/49404-exacta-mix-vented-micro-volume-inlet-recall-incorrect-filter-may. Based on FDA recall #Z-2262-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2262-2026%22&limit=1).
Baxter Healthcare Corporation voluntarily recalled its Exacta Mix Vented Micro-Volume Inlet tubing sets due to the risk of incorrect filters, the FDA said on April 22, 2026. The agency issued recall number Z-2262-2026 for the Class II device.
How to tell if you have it
Brand: Exacta Mix
Product Name: Vented Micro-Volume Inlet
Model/Catalog Number: H938175
Lot Codes: 804084, 804088, and 804089
UDI Number: 00085412475806
The hazard
Affected lots may contain incorrect 0.8-micron filters instead of the validated 3-micron filter, potentially causing reduced flow efficiency or system alarms. This issue may lead to clinical effects such as electrolyte imbalance, metabolic instability, or delayed recovery.
Context
GovInfoNow's records show Baxter Healthcare Corporation has 187 other recalls on record since September 2, 2015. Other recent recalls of similar products include Fresenius 5008X Blood Tubing Set (May 11, 2026), B Braun ULTRASITE IV Sets (October 29, 2025), and B Braun Blood Administration Sets (October 29, 2025).
How to tell if you have this one
Check for model number H938175 on the tubing sets. Affected lots include 804084, 804088, and 804089. The UDI number is 00085412475806.
Brand
Exacta Mix
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Filter Type
Verify that the filter is a validated 3-micron filter, not a 0.8-micron filter.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 43 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA 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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arizona, Arkansas, California, Colorado, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 49 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-2262-2026 (April 22, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2262-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.