Recall of Philips Respironics Trilogy Evo Universal Ventilator
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Philips Respironics is recalling 113,717 units of its Trilogy Evo Universal ventilator due to a potential delay in the obstruction alarm, which may not trigger within required standards.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 15, 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.
Recall Article
What Happened
Philips Respironics, Inc. has initiated a voluntary recall for the Trilogy Evo Universal ventilator because in some situations, the Obstruction Alarm does not trigger within the timeframe dictated by relevant standards and may take up to four breaths.
Which Products Are Affected
The affected products are the Philips Respironics Trilogy Evo Universal with Software Version 1.05.15.00. This recall involves 113,717 units, affecting all model numbers, all UDIs, and all serial numbers. The products were distributed nationwide in the United States.
What You Should Do
Consumers with the affected device should contact Philips Respironics for instructions, as the recall was initiated via letter. The firm's address is 1001 Murry Ridge Ln, Murrysville, PA 15668-8517.
Why This Matters
This recall is significant as it involves a Class I classification, indicating a potential for serious health risks due to the alarm malfunction in a continuous home-use ventilator device.
Source
Attribution: FDA. For more information, refer to the FDA recall with event ID 98540.
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 (1,114 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to April 15, 2026.
Frequently Asked Questions
Common questions about this FDA recall.