Hillrom VOLARA System P.CIRCUIT KIT Recall Issued
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Baxter Healthcare Corporation is recalling 10,540 units of the Hillrom VOLARA System P.CIRCUIT KIT due to reports of air and medication leakage from the nebulizer cup.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 8, 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, medical-devices.
What Happened
Baxter Healthcare Corporation initiated a voluntary recall of the Hillrom VOLARA System P.CIRCUIT KIT after reports of air and medication leakage from the nebulizer cup during therapy. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, affecting delivery of the prescribed treatment. The issue is associated with improper locking of the nebulizer cup after adding medication.
Which Products Are Affected
The recall affects the Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085. UDI: 00887761985018. All lot numbers distributed beginning on 4/28/2025. A total of 10,540 units are involved. Distribution was nationwide in the United States and Canada.
What You Should Do
Consumers should follow the recall instructions provided by Baxter Healthcare Corporation regarding the affected devices.
Why This Matters
This Class I recall addresses a defect that may reduce oxygen levels and compromise prescribed respiratory therapy.
Source
FDA recall number Z-2548-2026 (event ID 99119).
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 (1,098 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 8, 2026.
Frequently Asked Questions
Common questions about this FDA recall.