Baxter Duo-Vent Solution Set Recall Issued
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Baxter Healthcare Corporation is recalling 24,528 units of Baxter Duo-Vent Solution Set and Male Luer Lock Adapter due to reports of air bubbles in the drip chamber and tubing.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 25, 2026 and geographically references United States. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Baxter Healthcare Corporation initiated a voluntary recall after receiving customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position.
Which Products Are Affected
The recall covers Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets. A total of 24,528 units distributed nationwide in the United States are affected. Affected lot numbers include DR26C27062 (exp. 30-MAR-2028), DR26D14031 (exp. 15-Apr-2028), and DR26E13055 (exp. 14-May-2028). The UDI/DI is 00085412014319. The FDA recall number is Z-2766-2026 and the classification is Class I.
What You Should Do
Consumers should refer to the recalling firm for information on the affected products.
Why This Matters
This Class I recall involves a device distributed across the United States with a potential for serious adverse health consequences.
Source
https://www.fda.gov (Event ID: 99343, Recall Number: Z-2766-2026)
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,052 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 25, 2026.
Frequently Asked Questions
Common questions about this FDA recall.