Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alaris EtCO2 Recalled by CareFusion 303, Inc. Due to Calibration; it has been determined that the capnographs...
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 CareFusion 303, Inc. directly.
Affected Products
Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933
Quantity: 76 EtCO2 units
Why Was This Recalled?
Calibration; it has been determined that the capnographs may have been calibrated during manufacturing using a lower than specified concentration of CO2
Where Was This Sold?
This product was distributed to 10 states: CA, IL, IA, KS, KY, MN, NC, SD, TX, DC
About CareFusion 303, Inc.
CareFusion 303, Inc. has 163 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report