FDAFDA · Food and drugs·Recall number Z-2089-2013
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.
Published September 4, 2013 · Recall initiated: July 22, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- MCKESSON TECHNOLOGIES INC
- Distributor
- USA Nationwide Distribution in the states AR, MD, NJ, NY, PA, and WV.
- Lot
- Model Number (software version) 8.0.2 & 8.0.1 with RapiDispense
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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