Reported Sep 4, 2013 · Terminated
Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product Usage: Automated anesthesia cart that…
Mckesson Technologies Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MCKESSON TECHNOLOGIES INC · 5995 Windward Pkwy · Alpharetta, GA · 30005-4184
Is this the product you have?
- Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1
- with RapiDispense Product UsageAutomated anesthesia cart that monitors and controls the dispensing of medications, narcotics and supplies during surgical procedures
- Lot codes and dates
- Model Number (software version) 8.0.2 & 8.0.1 with RapiDispense
- Amount recalled
- 106
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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