Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Invacare Perfecto 2 V Oxygen Concentrator The finished device is Recalled by Invacare Corporation Due to It was determined that a defective sieve bed...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Invacare Corporation directly.
Affected Products
Invacare Perfecto 2 V Oxygen Concentrator The finished device is packaged as a single unit. The service part contains a single pair of sieve beds; one pair of sieve beds is used in a single finished device. Intended to provide supplemental oxygen to patients with respiratory disorders, by separating nitrogen from room air, by way of a molecular sieve.
Quantity: 5,963
Why Was This Recalled?
It was determined that a defective sieve bed subassembly enabled zeolite sieve dust from the sieve beds to migrate into the valves of the manifold assembly and muffler causing a reduction in oxygen concentration.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Invacare Corporation
Invacare Corporation has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report