Mc Kesson Anesthesia-Rx Model Number 8 — Class II medical device recall Z-2089-2013
Terminated recall by MCKESSON TECHNOLOGIES INC, reported 2013-09-04, distributed nationwide. The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted
| Recall number | Z-2089-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MCKESSON TECHNOLOGIES INC, Alpharetta, GA, United States |
| Recall initiated | 2013-07-22 |
| Classified | 2013-08-26 |
| Reported by FDA | 2013-09-04 |
| Terminated | 2014-06-19 |
| Distributed | Nationwide (US) |
| Quantity | 106 |
| Model numbers | 8.0.1, 8.0.2 |
Product
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.
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2089-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.