Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring Recalled by Covidien LP (formerly Nellcor Puritan Bennett Inc.) Due to Potential missing segments on the display that can...
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 Covidien LP (formerly Nellcor Puritan Bennett Inc.) directly.
Affected Products
OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring of functional arterial oxygen saturation (SpO2) and pulse rate.
Quantity: 105,831 units
Why Was This Recalled?
Potential missing segments on the display that can result in misinterpretation of data.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien LP (formerly Nellcor Puritan Bennett Inc.)
Covidien LP (formerly Nellcor Puritan Bennett Inc.) has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report