Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Recalled by MCKESSON TECHNOLOGIES INC Due to The firm issued a clinical alert after users...
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 TECHNOLOGIES INC directly.
Affected Products
Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product Usage: Automated anesthesia cart that monitors and controls the dispensing of medications, narcotics and supplies during surgical procedures.
Quantity: 106
Why Was This Recalled?
The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MCKESSON TECHNOLOGIES INC
MCKESSON TECHNOLOGIES INC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report