MCKESSON TECHNOLOGIES INC: Medical Device Recall in 2013 - (Recall #: Z-2089-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: July 22, 2013

Date Posted: September 4, 2013

Recall Number: Z-2089-2013

Event ID: 65769

Reason for Recall:

The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.

Status: Terminated

Product Quantity: 106

Code Information:

Model Number (software version) 8.0.2 & 8.0.1 with RapiDispense

Distribution Pattern:

USA Nationwide Distribution in the states AR, MD, NJ, NY, PA, and WV.

Voluntary or Mandated:

Voluntary: Firm initiated