Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component Recalled by Nellcor Puritan Bennett Inc. (dba Covidien LP) Due to In the case of a loss of GUI...
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 Nellcor Puritan Bennett Inc. (dba Covidien LP) directly.
Affected Products
Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component of the Puritan Bennett 840 Ventilator: The Backlight Inverter Printed Circuit Board (BLI PCBA) for the 9.4 Display part number 4-079056-00. The PB840 Ventilator System is intended to provide invasive or non-invasive ventilator support and monitoring for infant, pediatric, and adult patients with respiratory failure or respiratory insufficiency. It is used in hospitals and healthcare facilities
Quantity: 7371
Why Was This Recalled?
In the case of a loss of GUI display due to a Backlight Inverter PCBA failure, the ventilator continues to provide uninterrupted ventilatory support at the programmed settings for the patient. However, there is a loss of display and thus there is a necessity to move the patient to another ventilator.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Nellcor Puritan Bennett Inc. (dba Covidien LP)
Nellcor Puritan Bennett Inc. (dba Covidien LP) has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report