Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete Recalled by Mckesson Information Solutions LLC Due to McKesson Cardiology Hemo front-end parameter boxes must undergo...
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 Mckesson Information Solutions LLC directly.
Affected Products
McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.
Quantity: 625 devices
Why Was This Recalled?
McKesson Cardiology Hemo front-end parameter boxes must undergo annual maintenance testing to establish the proper functioning of the parameter boxes, and to identify in a timely manner whether a parameter box is out of calibration. McKesson has identified that its communication to customers regarding the required maintenance tests was insufficient. While each unit has an attached sticker i
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mckesson Information Solutions LLC
Mckesson Information Solutions LLC has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report