Lower riskMedical device recall · FDA · Published December 20, 2024
Baxter Continu-Flo Solution Set Recall: Inverted Clamps Cause Tubing Failure
Baxter recalls specific lots of Continu-Flo Solution Sets with Duo-Vent Spike due to inverted side clamps that can make tubing unusable. Affected units have lot numbers DR24B21017 (expiring 02/28/2026).
“Baxter Continu-Flo Solution Set Recall: Inverted Clamps Cause Tubing Failure.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53183-baxter-continu-flo-solution-set-recall-inverted-clamps-cause-tubing. Based on FDA recall #Z-1011-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1011-2025%22&limit=1).
Baxter Healthcare Corporation is voluntarily recalling specific lots of the Baxter Continu-Flo Solution Set with Duo-Vent Spike due to potential inverted side clamps that render the tubing unusable, the FDA said on December 20, 2024.
How to tell if you have it
Brand: Baxter
Product: Baxter Continu-Flo Solution Set with Duo-Vent Spike
REF: UC8519
UDI/DI: 00085412486512
Lot Numbers: DR24B21017 (exp. 02/28/2026)
Distribution: US Nationwide in MN, MO, VA, TX, CA, MA, FL, SC
The hazard
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
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 ICU Medical CADD Yellow Medication Cassette Reservoir Recall (August 20, 2026), Medline Nerve Block Trays Recall (April 27, 2026), and Medline ENFIT G-TUBE Connector Recall (February 13, 2026).
How to tell if you have this one
Check for the lot number DR24B21017 on the product packaging, which expires on 02/28/2026. The product is part of the Baxter Continu-Flo Solution Set with Duo-Vent Spike, reference number UC8519.
Brand
Baxter
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution in the states of MN, MO, VA, TX, CA, MA, FL, SC.
Recall number
Product, codes & lots
Quantity
Z-1009-2025
Baxter Solution Set with Duo-Vent Spike, REF 2R8404; UDI/DI 00085412676630, Lot Numbers: DR24C22079 (exp.3/247/2026), DR24H23086 (exp. 8/26/2026)
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Z-1010-2025
Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538; UDI/DI 00085412676647, Lot Numbers: DR24C15109 (exp. 3/16/2026)
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Z-1011-2025
Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519; UDI/DI 00085412486512, Lot Numbers: DR24B21017 (exp. 02/28/2026)
—
Based on the official FDA remedy
What to do — step by step
Check Product Lot Number
Look for the lot number DR24B21017 on the packaging to confirm if your unit is affected.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 8 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of MN, MO, VA, TX, CA, MA, FL, SC.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Florida, Massachusetts, Minnesota, Missouri, South Carolina, Texas, Virginia.
Recall timeline
FDA published this recall 40 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-1011-2025 (December 20, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1011-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.